HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902233Generated: October 30, 2026
Pyridine → N-propyl-N-propoxy-bromoacetamide
https://huagongshe.com/reaction/902233
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | N-Propyl-N-propoxyamine hydrochloride | HCID 22322517 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-propyl-N-propoxy-bromoacetamide | HCID 22322784 | 197.8% |
Reaction Steps
N-Propyl-N-propoxyamine hydrochloride (0.30 g) was dissolved in acetonitrile and cooled to −20° C. Pyridine (0.2 mL) was added. Bromoacetyl bromide (0.15 g) was added dropwise over 5 min. The solution was stirred at −20° C. for 30 min. The bath was removed and the solution was stirred for 6 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 (0.35 g). The product is a mixture of chloro- and bromoacetamides in a ratio of ˜3:1.
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-d0547400d0eb4071a58bf9ea759b6596 |
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| Source note | uspto-grants-2008_04 |
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