HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053706Generated: October 31, 2026
Bis(2-chloroethyl)carbamoyl chloride → tert-Butyl 3-[5-[bis(2-chloroethyl)carbamoyloxy]-2-methyl-phenyl]-4-(tert-butoxycarbonylamino)butanoate
https://huagongshe.com/reaction/1053706
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bis(2-chloroethyl)carbamoyl chloride | HCID 76346 | — |
| Reactant | tert-Butyl 4-(tert-butoxycarbonylamino)-3-(5-hydroxy-2-methyl-phenyl)butanoate | HCID 118277046 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | tert-Butyl 3-[5-[bis(2-chloroethyl)carbamoyloxy]-2-methyl-phenyl]-4-(tert-butoxycarbonylamino)butanoate | HCID 118276980 | — |
Reaction Steps
Adapting a literature known protocol (U.S. Pat. No. 3,299,104), tert-butyl 3-[5-[bis(2-chloroethyl)carbamoyloxy]-2-methyl-phenyl]-4-(tert-butoxycarbonylamino)butanoate (23e) is prepared through carbamoylation of tert-butyl 4-(tert-butoxycarbonylamino)-3-(5-hydroxy-2-methyl-phenyl)butanoate (23d) (731 mg, 2.0 mmol) with commercial N,N-bis(2-chloroethyl)carbamoyl chloride (439 μL, 614 mg, 3.0 mmol) in anhydrous pyridine (15 mL) at about 0° C. The reaction mixture is stirred with gradual warming to room temperature. The reaction is monitored by TLC and/or LC/MS to completion. Excess of the carbamoyl chloride is destroyed with crushed ice. Aqueous work-up followed by purification through silica gel column chromatography afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09394236B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-a24794b1426c42008815ef84bc34cf67 |
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| Source note | uspto-grants-2016_07 |
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