HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328625Generated: October 25, 2026
Triethylamine → N-(2-bromopropionyl)-2-chloro-6-methylbenzylamine
https://huagongshe.com/reaction/328625
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Propanoyl bromide, 2-bromo- | HCID 79047 | — |
| Reactant | 2-Chloro-6-methylbenzylamine | HCID 521799 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | N-(2-bromopropionyl)-2-chloro-6-methylbenzylamine | HCID 21442921 | — |
Reaction Steps
A mixture of 35 parts of 2-chloro-6-methylbenzylamine and 30 parts of triethyl amine in 400 parts of ethylene chloride is stirred and cooled to -35°C. While keeping the temperature between -35° and -20° C., there is added dripwise a solution of 50 parts of 2-bromopropionyl bromide in 160 parts of ethylene chloride. Upon completion, the whole is stirred for one hour at room temperature. The reaction mixture is washed with diluted hydrochloric acid and once with water. The organic phase is dried over magnesium sulfate, filtered and evaporated. The solid residue is crystallized from a mixture of 400 parts of ethanol and 150 parts of water, yielding 40 parts of N-(2-bromopropionyl)-2-chloro-6-methylbenzylamine; mp. 168° -169° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04017631 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-1b6ce62300c14f95ac4f7a59af9136f3 |
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| Source note | uspto-grants-1977_04 |
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