4-(Methylsulfonyl)phenol CAS 14763-60-1

Introduction:Basic information about 4-(Methylsulfonyl)phenol CAS 14763-60-1, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

4-(Methylsulfonyl)phenol Basic information

Product Name:4-(Methylsulfonyl)phenol
Synonyms:4-(METHYLSULFONYL)PHENOL;4-METHYLSULPHONYLPHENOL;4-METHANESULFONYL-PHENOL;4-(methylsulfonyl)-pheno;4-Hydroxyphenyl methyl sulfone;4-hydroxyphenylmethylsulfone;p-(methylsulfonyl)-pheno;p-(Methylsulfonyl)phenol
CAS:14763-60-1
MF:C7H8O3S
MW:172.2
EINECS:632-596-9
Product Categories:
Mol File:14763-60-1.mol

4-(Methylsulfonyl)phenol Chemical Properties

Melting point 90-95 °C
Boiling point 272.52°C (rough estimate)
density 1.3692 (rough estimate)
refractive index 1.5151 (estimate)
RTECS SM1530000
storage temp. Inert atmosphere,Room Temperature
solubility DMSO, Methanol
form Powder
pkapK1:7.83 (25°C)
color Tan to pink-brown
Water Solubility slight
BRN 1866322
LogP0.886 (est)
CAS DataBase Reference14763-60-1(CAS DataBase Reference)
NIST Chemistry Reference4-(Methylsulfonyl)phenol(14763-60-1)

Safety Information

Hazard Codes Xi
Risk Statements 36
Safety Statements 24/25-26
WGK Germany 3
Hazard Note Irritant
HS Code 29309090

4-(Methylsulfonyl)phenol Usage And Synthesis

Chemical PropertiesTan to pink-brown powder
Uses4-(Methylsulfonyl)phenol is a reagent in the synthesis of pyrazolo[3,4-d]pyrimidine derivatives as GPR119 agonists. Also a reagent in the synthesis of novel 2-(pyridine-2-yl)-1H-benzimidazole derivatives as potent glucokinase activators.
ReactionsThe reaction of 4-(methylsulfonyl)phenol (17.2 g, 100.0 mmol) with p-Toluenesulfonic anhydride as outlined in the general procedure provided 4-(methylsulfonyl)phenyl 4-methylbenzenesulfonate (26.1 g, 81%).
Synthesis

1073-72-9

14763-60-1

Step 2. Synthesis of 4-(methylsulfonyl)phenolOxone (0.99 g, 6.5 mmol) was added batchwise to a solution of 4-(methylthio)phenol (0.50 g, 3.2 mmol) in ethanol (10.0 mL). Subsequently, water (10.0 mL) was added at room temperature. The reaction mixture was stirred for 18 h, after which it was partitioned between ethyl acetate and water. The combined organic layers were washed with brine, dried over magnesium sulfate, and concentrated under vacuum to afford 4-(methylsulfonyl)phenol as a semi-solid (0.60 g, 96% yield).LCMS calculated value C7H9O3S ([M + H]+): m/z = 173.0; measured value: 173.0.

References[1] Patent: WO2015/164480, 2015, A1. Location in patent: Page/Page column 106; 107
[2] Journal of Organic Chemistry, 2003, vol. 68, # 13, p. 5388 - 5391
[3] Green Chemistry, 2014, vol. 16, # 4, p. 2190 - 2196
[4] Journal of the Indian Chemical Society, 1982, vol. 59, # 1, p. 52 - 54
[5] Patent: EP1598349, 2005, A1. Location in patent: Page/Page column 127

4-(Methylsulfonyl)phenol Preparation Products And Raw materials

Raw materialsSodium hydroxide-->Hydrochloric acid-->Ethyl acetate-->Acetic acid-->Chloroform-->Magnesium sulfate-->Hydrogen peroxide-->Carbon tetrachloride-->Acetyl chloride-->Sodium periodate-->4-(Methylthio)phenol
Preparation Products2-BROMO-4-(METHYLSULFONYL)PHENOL-->1-(2-bromoethoxy)-4-(methylsulfonyl)benzene
4-(METHYLAMINO)-3-NITROBENZOIC ACID CAS 41263-74-5
4-(METHYLSULFONYLAMINO)PHENYLBORONIC ACID CAS 380430-57-9
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