HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946902Generated: October 31, 2026
Chloroacetyl chloride → N-[1-(3-Bromophenyl)-2-hydroxy-1-methylethyl]-2-chloroacetamide
https://huagongshe.com/reaction/1946902
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-2-(3-bromophenyl)propan-1-ol | HCID 53256694 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-[1-(3-Bromophenyl)-2-hydroxy-1-methylethyl]-2-chloroacetamide | HCID 58155284 | 87.2% |
Reaction Steps
A solution of crude (RS)-2-amino-2-(3-bromo-phenyl)-propan-1-ol (8.38 g, 36 mmol) and triethylamine (6.08 ml, 44 mmol) in acetonitrile (140 ml) was treated dropwise at −2° C. with chloro-acetyl chloride (3.25 ml, 40 mmol). After complete addition, the orange colored solution was left to warm to room temperature and stirring was continued for 2 h. For the workup, to the reaction was added silica gel (10 g) and it was evaporated at reduced pressure, thereafter, it was purified by chromatography on silica gel using a gradient of dichloromethane/methanol=100/0 to 90/10 as the eluent. There were obtained 9.62 g (86% of theory) of (RS)—N-[1-(3-bromo-phenyl)-2-hydroxy-1-methyl-ethyl]-2-chloro-acetamide as a light brown oil. MS (ISP): m/z=304.1 [M+H]+, 306.1 [M+2+H]+, 308.2 [M+4+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399459B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-1f06a2306cce4713820db28917993c36 |
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| Source note | uspto-grants-2013_03 |
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