HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1105895Generated: October 26, 2026
Chloroform → 4-[N-carbobenzyloxy-15-(trifluoromethyl)pentadecylamino]benzoyl chloride
https://huagongshe.com/reaction/1105895
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 4-[15-(Trifluoromethyl)pentadecylamino]benzoic acid | HCID 12831610 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[N-carbobenzyloxy-15-(trifluoromethyl)pentadecylamino]benzoyl chloride | HCID 12831611 | — |
Reaction Steps
To 15 g. 4-[15-(trifluoromethyl)pentadecylamino]benzoic acid in 200 ml. warm chloroform is added a solution of 15 g. of 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 1 N hydrochloric acid, dried, and evaporated 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-15-(trifluoromethyl)pentadecylamino]benzoyl chloride as a viscous, orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04310545 |
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| Source dataset | uspto-grants-1982_01 |
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| ORD ID | ord-5aecfa93a1294bfa904246ef187fdedc |
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| Source note | uspto-grants-1982_01 |
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