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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 22322684 | HCID 22322684 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | n-Butyl-n-propoxy-bromoacetamide | HCID 22322793 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07365093B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-3220bbd4ed5a47759374df9172aea477 |
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| Source note | uspto-grants-2008_04 |
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