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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9082Generated: October 25, 2026

Triethylamine → 8-Bromo-octanoic acid benzyloxyamide

https://huagongshe.com/reaction/9082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyloxyamine hydrochlorideHCID 102312—
ReactantBis(2-oxo-3-oxazolidinyl)phosphinic chlorideHCID 152842—
Reactant8-Bromooctanoic acidHCID 548275—
SolventDichloromethaneHCID 6344—
Product8-Bromo-octanoic acid benzyloxyamideHCID 1133640378%

Reaction Steps

In an ice bath, 14 ml triethylamine was added to a suspension of 3.2 g (20 mmol) O-benzylhydroxylamine hydrochloride in 150 ml dichloromethane. Stirring was continued until the solution became clear. Then, 4.5 g (20 mmol) 8-bromo octanoic acid was added, followed by 5.6 g (22 mmol) bis-(2-oxo-3-oxazolidinyl)-phosphorylchloride. Stirring was continued at ambient temperature for 18 h. The solution was extracted twice with 150 ml each of 1M aqueous hydrochloric acid and twice with 150 ml each of 1M aqueous sodium bicarbonate. The organic solvent was removed i. vac. to give 5.1 g (78%) of 8-bromo-octanoic acid benzyloxyamide as a colorless oil. MS: 330 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091229B2
Source datasetuspto-grants-2006_08
ORD IDord-1345b2679a1f4255af5f660665af3050
Source noteuspto-grants-2006_08