Ethyl diazoacetate CAS 623-73-4

Introduction:Basic information about Ethyl diazoacetate CAS 623-73-4, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Ethyl diazoacetate Basic informationSynthesis

Product Name:Ethyl diazoacetate
Synonyms:Acetic acid, diazo-, ethyl ester;Daae;Diazoacetic acid ethyl ester;Diazoacetic ester;diazoaceticacid,ethylester;diazo-aceticaciethylester;diazoaceticester;Diazoessigsaeure-aethylester
CAS:623-73-4
MF:C4H6N2O2
MW:114.1
EINECS:210-810-8
Product Categories:Azo/Diazo Compounds;Building Blocks;Carboxylic;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks;Azo/Diazo Compounds;Nitrogen Compounds;Organic Building Blocks
Mol File:623-73-4.mol

Ethyl diazoacetate Chemical Properties

Melting point -22 °C (lit.)
Boiling point 140-141 °C/720 mmHg (lit.)
density 1.085 g/mL at 25 °C (lit.)
refractive index n20/D 1.46(lit.)
Fp 115 °F
storage temp. 2-8°C
solubility Chloroform (Slightly), DMSO (Soluble), Hexane (Slightly), Methanol (Slightly)
form Oil
color Light Yellow to Orange
Merck 13,3021
BRN 107654
InChIInChI=1S/C4H6N2O2/c1-2-8-4(7)3-6-5/h3H,2H2,1H3
InChIKeyYVPJCJLMRRTDMQ-UHFFFAOYSA-N
SMILESC(=O)(OCC)C=[N+]=[N-]
NIST Chemistry ReferenceEthyl diazoacetate(623-73-4)

Safety Information

Hazard Codes Xn,F
Risk Statements 5-10-22-40-67-65-48/20-38-11-63
Safety Statements 36/37-62-16
RIDADR UN 1993 3/PG 3
WGK Germany 3
RTECS AG5775000
HazardClass 3.2
PackingGroup III
HS Code 29270000
Storage Class5.2 - Organic peroxides and self-reacting hazardous materials
Hazard ClassificationsAcute Tox. 4 Oral
Carc. 2
Eye Irrit. 2
Flam. Liq. 3
Self-react. E
Skin Irrit. 2

Ethyl diazoacetate Usage And Synthesis

SynthesisGlycine ethyl ester hydrochloride can be dissolved in a buffer solution composed of acetic acid and sodium acetate, and then dichloroethane is added as a solvent, and sodium nitrite solution is added dropwise at 10 to 15 ° C. After the dropwise addition, continue stirring for 15min. The separated organic layer is a dichloroethane solution of ethyl diazoacetate.
NH2CH2COOC2H5·HCl+NaNO2+HCl→N2CHCOOC2H5+NaCl+H2O
Chemical PropertiesLiquid.
UsesReagent for ruthenium-catalyzed asymmetric cyclopropanation of alkenes.1
UsesNew Diazoacetate Formulations
HazardFlammable liquid that explodes whenheated.
Safety ProfilePoison by ingestion and intravenous routes. Questionable carcinogen with experimental carcinogenic and tumorigenic data. Can explode. Explodes on contact with tris(dimethy1amino) antimony. When heated to decomposition it emits toxic fumes of NOx. See also ESTERS.
Purification MethodsIt is a very volatile yellow oil with a strong pungent odour. EXPLOSIVE [distillation even under reduced pressure is dangerous and may result in an explosion — TAKE ALL THE NECESSARY PRECAUTIONS IF DISTILLATION IS TO BE CARRIED OUT]. It explodes in contact with conc H2SO4-trace acid causes rapid decomposition. It is slightly soluble in H2O, but is miscible with EtOH, *C6H6, pet ether and Et2O. To purify, dissolve it in Et2O [using CH2Cl2 instead of Et2O, protects the ester from acid], wash it with 10% aqueous Na2CO3, dry (MgSO4), filter and repeat as many times as possible until the Et2O layer loses its yellow colour, then remove the solvent below 20o (vacuum). Note that prolonged heating may lead to rapid decomposition and low yields. It can also be purified by steam distillation under reduced pressure but with considerable loss in yield. Place the residual oil in a brown bottle, keep below 10o, and use as soon as possible without distilling. For preparing esters usually the ethereal solution is used directly without purification. [Womack & Nelson Org Synth Coll Vol III 392 1955, UV: Miller & White J Am Chem Soc 79 5974 1957, Fieser 1 367 1967, Beilstein 3 IV 1495.]

Ethyl diazoacetate Preparation Products And Raw materials

Raw materialsEthyl acetate-->Glycine ethyl ester hydrochloride-->Permethric acid-->Buffer solution, pH 1.00 (±0.01 at 25°C), No Color, Specpure, NIST Traceable
Preparation ProductsEthyl chrysanthemumate-->2,2-Dimethyl-3-(2-methylpropyl)cyclopropanecarboxylic acid p-(methoxymethyl)benzyl ester-->ethyl glycinate-->Ethyl glycolate-->Benzeneacetic acid, α-(hydroxymethylene)-, ethyl ester, (αZ)--->Heptanoic acid, 2-methyl-3-oxo-, ethyl ester-->2-Pentenedioic acid, diethyl ester, (Z)- (9CI)-->2-Oxiranecarboxylicacid, 3-(trichloromethyl)-, ethyl ester-->ETHYL 3-BUTYNOATE-->ETHYL 3-METHOXYPHENYLACETATE-->Ethyl 4-methoxycinnamate-->2-HYDROXYMETHYL-CYCLOPROPANECARBOXYLIC ACID ETHYL ESTER-->Diethyl iminodiacetate-->ethyl 5-(hydroxymethyl)-1H-pyrazole-3-carboxylate
Ethyl crotonate CAS 623-70-1
Ethyl dichlorophosphate CAS 1498-51-7
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