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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49516Generated: October 29, 2026

Water → 6-Fluoro-5-(5-hydroxy-pent-1-ynyl)-2,3-dihydro-indole-1-carboxylic acid 4-chloro-phenyl ester

https://huagongshe.com/reaction/49516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Chlorophenyl chloroformateHCID 139059—
Reactant5-(6-Fluoro-2,3-dihydro-1H-indol-5-yl)-pent-4-yn-1-olHCID 21966615—
SolventDichloromethaneHCID 6344—
Product6-Fluoro-5-(5-hydroxy-pent-1-ynyl)-2,3-dihydro-indole-1-carboxylic acid 4-chloro-phenyl esterHCID 6951512474.3%

Reaction Steps

A solution of 99 mg (0.45 mmol) 5-(6-Fluoro-2,3-dihydro-1H-indol-5-yl)-pent-4-yn-1-ol and 0.155 ml (0.90 mmol) N-Ethyldiisopropylamine in 2 ml CH2Cl2 was treated with 0.125 ml (0.90 mmol) 4-chlorophenyl chloroformate and stirred at room temperature during 1 hour. The mixture was poured into water, extracted with EtOAc and the combined organic layers were dried with MgSO4. Evaporation of the solvent, chromatography on silica gel with CH2Cl2/MeOH 49:1 gave 125 mg (74%) of 6-Fluoro-5-(5-hydroxy-pent-1-ynyl)-2,3-dihydro-indole-1-carboxylic acid 4-chloro-phenyl ester as a viscous light yellow oil, MS: 374 (MH+, 1Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706751B2
Source datasetuspto-grants-2004_03
ORD IDord-e2ae7ee208414766bb56c59d43ca13d5
Source noteuspto-grants-2004_03