Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973301Generated: October 30, 2026

Borane → 5-Chloro-2-(2-hydroxyethyl)-3-phenylisoindole-1-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1973301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoraneHCID 6331—
Reactant1-Ethoxycarbonyl-5-chloro-3-phenylisoindole-2-acetic acidHCID 20351800—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-2-(2-hydroxyethyl)-3-phenylisoindole-1-carboxylic acid ethyl esterHCID 54432893—

Reaction Steps

A solution of 10.8 g. of 1-ethoxycarbonyl-5-chloro-3-phenylisoindole-2-acetic acid in 100 ml. of tetrahydrofuran is added dropwise under argon at 15°-20° C. to 72 ml. of a 1-M solution of borane in tetrahydrofuran. After stirring at room temperature for 60 hours, the clear solution is treated at 15°-20° C. with 30 ml. of ethanol and evaporated to dryness under reduced pressure. The solid residue is dissolved in methylene chloride and the obtained solution washed with a 5% sodium bicarbonate solution and then with water. The solution is dried over sodium sulfate, evaporated and the solid crude product obtained chromatographed on 700 g. of silica gel with methylene chloride/ethyl acetate (4:1) as the eluant. The uniform fractions yield 5-chloro-2-(2-hydroxyethyl)-3-phenylisoindole-1-carboxylic acid ethyl ester; melting point 114°-116° C. Recrystallization from ether/pentane does not increase the melting point.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03996374
Source datasetuspto-grants-1976_12
ORD IDord-e80f53d92a4c4c7da5651100f53800ab
Source noteuspto-grants-1976_12