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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986404Generated: October 30, 2026

Boron tribromide → HCID 28303003, compound

https://huagongshe.com/reaction/1986404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
Reactant3-Methoxy-N-[2-(4-morpholinyl)ethyl]benzenesulfonamideHCID 68875424—
SolventDichloromethaneHCID 6344—
ProductHCID 28303003HCID 28303003—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of boron tribromide (1M in CH2Cl2, 20 mL, 20 mmol) was added to a −78° C. solution of the product of Step 1 in CH2Cl2 (50 mL) and the resulting mixture was allowed to warm to 0° C. After 2 h at 0° C. the mixture was re-cooled to −78° C. and quenched with sat. aq. NaHCO3 solution and allowed to warm to rt. The mixture was extracted with EtOAc, and the organic layers was washed with H2O and brine, dried (MgSO4), filtered and the filtrate was concentrated to give the title compound as a crude oil (1.9 g, 66%) which was used directly in the next step. MS (ES+) m/e 287 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547779B2
Source datasetuspto-grants-2009_06
ORD IDord-ef4fbb232fd8499db0bd9af17d59eba5
Source noteuspto-grants-2009_06