Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902239Generated: October 28, 2026

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

https://huagongshe.com/reaction/902239

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 numberUS07365093B2
Source datasetuspto-grants-2008_04
ORD IDord-3220bbd4ed5a47759374df9172aea477
Source noteuspto-grants-2008_04