HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278302Generated: November 1, 2026
Chloroform → 4-(N-carbobenzyloxy-allylamino)phenylacetyl chloride
https://huagongshe.com/reaction/1278302
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Acetic acid, 2-(p-(allylamino)phenyl)- | HCID 38316 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(N-carbobenzyloxy-allylamino)phenylacetyl chloride | HCID 54085438 | — |
Reaction Steps
To 15 g. 4-(allylamino)phenylacetic acid in 200 ml. warm chloroform is added a solution of 12 g. sodium carbonate in 150 ml. water. To the vigorously stirred solution is added 10 g. carbobenzyloxy chloride. After 2 hours stirring at 40° C., the layers are separated, washed three times with 1N hydrochloric acid, dried, and evaorated to an oil. The oil is dissolved in 300 ml. toluene, treated with 15 ml. thionyl chloride and the solution is refluxed for 5 hours. The solvents are evaporated and the residue is dissolved three times in toluene, evaporating each time ultimately to yield 4-(N-carbobenzyloxy-allylamino)phenylacetyl chloride as a viscous, orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04281019 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-4801e610fd864cbc99ef41ee1f028d61 |
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| Source note | uspto-grants-1981_07 |
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