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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973302Generated: October 26, 2026

Triethylamine → 5-Chloro-2-{2-[(methylsulfonyl)oxy]ethyl}-3-phenylisoindole-1-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1973302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethane sulfochlorideHCID 19821184—
Reactant5-Chloro-2-(2-hydroxyethyl)-3-phenylisoindole-1-carboxylic acid ethyl esterHCID 54432893—
SolventDichloromethaneHCID 6344—
Product5-Chloro-2-{2-[(methylsulfonyl)oxy]ethyl}-3-phenylisoindole-1-carboxylic acid ethyl esterHCID 53691054—

Reaction Steps

A solution of 3.4 g. of 5-chloro-2-(2-hydroxyethyl)-3-phenylisoindole-1-carboxylic acid ethyl ester and 3.4 ml. of triethylamine in 60 ml. of methylene chloride is treated dropwise at 15°-20° C. with 1.6 ml. of methane sulfochloride. The mixture is subsequently left standing for 30 minutes at room temperature, then diluted with methylene chloride to three times the volume. The solution is washed successively with water, 0.5-N hydrochloric acid, 5% sodium bicarbonate solution and again with water. After drying over sodium sulfate and evaporation of the solution, there is obtained 5-chloro-2-{2-[(methylsulfonyl)oxy]ethyl}-3-phenylisoindole-1-carboxylic acid ethyl ester; melting point 125°-127° C. Recrystallization from methylene chloride/hexane does not increase the melting point.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03996374
Source datasetuspto-grants-1976_12
ORD IDord-14a4a9ffb83949608bc0655576ac41a9
Source noteuspto-grants-1976_12