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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587876Generated: October 27, 2026

Boron tribromide → ethyl 1-benzyl-6-hydroxy-2,3-dihydro-1H-inden-2-ylcarbamate

https://huagongshe.com/reaction/587876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 66740684HCID 66740684—
SolventDichloromethaneHCID 6344—
Productethyl 1-benzyl-6-hydroxy-2,3-dihydro-1H-inden-2-ylcarbamateHCID 66740125—

Reaction Steps

To a stirred and cooled (−10° C.) solution of ethyl 1-benzyl-6-methoxy-2,3-dihydro-1H-inden-2-ylcarbamate (668 mg, 2.053 mmol) in dichloromethane (15 ml) under argon was added dropwise 1M tribromoborane (6.16 ml, 6.16 mmol) and stirred over night while the reaction mixture was allowed to warm up to room temperature. Poured into ice water, diluted with dichloromethane, separated organic layer and the aqueous layer was extracted twice with dichloromethane. The combined organic layers were washed subsequently with water, sodium bicarbonate and brine, dried, filtered and evaporated to obtain ethyl 1-benzyl-6-hydroxy-2,3-dihydro-1H-inden-2-ylcarbamate as a brown solid. m=620 mg (97%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227930B2
Source datasetuspto-grants-2016_01
ORD IDord-5d5e9374cd434b1498479010135a4a63
Source noteuspto-grants-2016_01