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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272556Generated: November 2, 2026

Bromoacetyl bromide → n-Butyl-n-propoxy-bromoacetamide

https://huagongshe.com/reaction/1272556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 22322684HCID 22322684—
SolventAcetonitrileHCID 6342—
Productn-Butyl-n-propoxy-bromoacetamideHCID 22322793—

Reaction Conditions

Temperature-20 °C

Reaction Steps

The salt of Example 538B (0.60 g) was dissolved in acetonitrile (5 mL) and cooled to −20° C. Hünig's base (5.5 mL) was added slowly. Bromoacetyl bromide (0.5 mL) was added dropwise over five minutes. The solution was stirred at −20° C. for 30 minutes. The bath was removed and the solution was stirred for six hours at room temperature. The solvent was removed in vocuo and the residue taken up in EtOAc (50 mL) and washed with water (1×25 mL), 1N phosphoric acid (3×25 mL), and brine (1×25 mL). The organic layer was dried with sodium sulfate and evaporated to give a dark orange oil (0.65 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208517B1
Source datasetuspto-grants-2007_04
ORD IDord-1896aefcf7494bfeab336f796d9e167c
Source noteuspto-grants-2007_04