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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069663Generated: October 31, 2026

Boron tribromide → HCID 52951573, compound

https://huagongshe.com/reaction/2069663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantMethyl 5-methoxy-2,3-dihydro-1H-indene-2-carboxylateHCID 53724337—
SolventDichloromethaneHCID 6344—
ProductHCID 52951573HCID 52951573—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 5-methoxy-2,3-dihydro-1h-indene-2-carboxylate (696) (2.35 g, 11.4 mmol) in anhydrous dichloromethane (40 mL) cooled to −78° C. was added boron tribromide (1.5 eq.). The reaction was allowed to stir at −78° C. for 30 minutes, 0° C. for 2 hours, and at room temperature overnight. The reaction mixture was cooled to 0° C. and quenched slowly with methanol. After stifling for 15 minutes a saturated sodium bicarbonate solution was added slowly to the mixture and allowed to stir at 0° C. for 30 minutes. Ethyl acetate was added and the layers were separated. The aqueous layer was extracted with ethyl acetate and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to afford methyl 5-hydroxy-2,3-dihydro-1H-indene-2-carboxylate (697).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299117B2
Source datasetuspto-grants-2012_10
ORD IDord-24616afecf3b48b486165193b22d4f3e
Source noteuspto-grants-2012_10