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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108740Generated: October 29, 2026

Boron tribromide → HCID 22627290, compound

https://huagongshe.com/reaction/1108740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 22627199HCID 22627199—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 22627290HCID 2262729074%

Reaction Conditions

Temperature-12 °C

Reaction Steps

To a solution of 1-(2-chlorobenzyl)-3-methoxyacetyl-2-propylindole-6-carboxamide (168 mg) in a mixture of dichloromethane (10 ml) and methanol (0.5 ml) was added 1M solution or boron tribromide in dichloromethane (2.5 ml) at -53° C. The reaction mixture was warmed gradually to -12° C. during 3 hours. Then 1M solution of boron tribromide in dichloromethane (2.5 ml) was added, and the mixture was stirred for 20 minutes at -12° C. The reaction mixture was diluted with water and extracted with 10% methanol in chloroform. The organic phase was washed with aqueous sodium bicarbonate, water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was crystallized from ethyl acetate and washed with hexane to give 1-(2-chlorobenzyl)-3-hydroxyacetyl-2-propylindole-6-carboxamide (120 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069156
Source datasetuspto-grants-2000_05
ORD IDord-9d50a0472ad044c6a31770632647e6dd
Source noteuspto-grants-2000_05