Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49495Generated: October 29, 2026

1,4-Dibromobutane → 5-(4-Bromo-butoxy)-2,3-dihydro-indole-1-carboxylic acid 4-chloro-phenyl ester

https://huagongshe.com/reaction/49495

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Hydroxy-2,3-dihydro-indole-1-carboxylic acid 4-chloro-phenyl esterHCID 69514915—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product5-(4-Bromo-butoxy)-2,3-dihydro-indole-1-carboxylic acid 4-chloro-phenyl esterHCID 6951535449.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

290 mg (1 mmol) 5-Hydroxy-2,3-dihydro-indole-1-carboxylic acid 4-chloro-phenyl ester in 5 ml acetone were treated with 320 mg (3 mmol) K2CO3 (powdered) and 0.23 ml (2 mmol) 1,4-dibromobutane. The suspension was stirred at 50° C. for 4 h, cooled to RT, and was diluted with ether and water. The aqueous phase was extracted with ether, the organic phases were washed with water and dried over Na2SO4. Column chromatography on silica gel with hexane/EtOAc 9:1 yielded 210 mg (49%) 5-(4-Bromo-butoxy)-2,3-dihydro-indole-1-carboxylic acid 4-chloro-phenyl ester as colorless solid, MS: 423 (M, 1Br, 1Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706751B2
Source datasetuspto-grants-2004_03
ORD IDord-a02a88f0a9fe4a9c8b454315f934328f
Source noteuspto-grants-2004_03