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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991298Generated: November 1, 2026

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

https://huagongshe.com/reaction/991298

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 vacuo 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 numberUS06462194B1
Source datasetuspto-grants-2002_10
ORD IDord-20ee396e61d54792b7fc685fdc5054cd
Source noteuspto-grants-2002_10