HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275998Generated: October 26, 2026
Pyridine → N-butyl-N-(3-hydroxymethylphenyl)-bromoacetamide
https://huagongshe.com/reaction/1275998
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | [3-(Butylamino)phenyl]methanol | HCID 22322603 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-butyl-N-(3-hydroxymethylphenyl)-bromoacetamide | HCID 22323007 | — |
Reaction Steps
To a solution of 3.42 g (19.2 mmol) of the compound of Example 532A in 20 ml toluene, was added 2.42 ml (30 mmol) pyridine. The mixture was cooled to 0° C.; 4.025 gm (20.0 mmol) of bromoacetyl bromide (diluted with 5 ml toluene) was added in a dropwise fashion. The reaction mixture was allowed to stir for 5 hours at 0° C. and then was allowed to warm to room temperature. Saturated potassium carbonate solution was added, and the mixture was stirred vigorously for 2 hours. The mixture was extracted with EtOAc; the organic layer was washed with 1N H3PO4, water, and brine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06162927 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-a12f475ab6d6437bb1d940f32dd67f4f |
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| Source note | uspto-grants-2000_12 |
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