Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473094Generated: October 26, 2026

Diethyl Ether → benzyl N-(5-bromo-2,3-dihydro-1H-inden-1-yl)carbamate

https://huagongshe.com/reaction/473094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantBenzyl chloroformateHCID 10387—
ReactantPotassium CarbonateHCID 11430—
Reactant5-bromo-2,3-dihydro-1H-inden-1-amineHCID 22228388—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Productbenzyl N-(5-bromo-2,3-dihydro-1H-inden-1-yl)carbamateHCID 6708808682.4%

Reaction Steps

To a vigorously stirred solution of 5-bromo-2,3-dihydro-1H-inden-1-amine (8.54 g, 40.3 mmol) and potassium carbonate (11.1 g, 80 mmol) in water (100 mL) and ethyl acetate (100 mL) was added benzyl chloroformate (7.56 g, 44.3 mmol). The reaction was stirred at rt overnight before being diluted with water (200 mL) and dichloromethane (200 mL). The organic phase was collected and the aqueous phase was extracted once more with dichloromethane (100 mL). The clear colourless organic layers were dried over sodium sulfate, filtered, and concentrated under reduced pressure to afford a white solid. The material was co-evaporated once with diethyl ether and the residue was triturated with diethyl ether. The white solid was collected by filtration and dried on air to afford the title compound as a white solid (11.5 g, 82%). MS (ESI): m/z [M+H]+ 347.0

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633237B2
Source datasetuspto-grants-2014_01
ORD IDord-4acdf977ef684dc1841282fcb0655c48
Source noteuspto-grants-2014_01