HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921670Generated: October 30, 2026
Allyl chloroformate → Tert-butyl 4-(1-allyloxycarbonylaminocyclopropyl)benzoate
https://huagongshe.com/reaction/1921670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl chloroformate | HCID 18052 | — |
| Reactant | Tert-butyl 4-(1-aminocyclopropyl)benzoate | HCID 59305811 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 4-(1-allyloxycarbonylaminocyclopropyl)benzoate | HCID 59305799 | — |
Reaction Steps
3 g of tert-butyl 4-(1-aminocyclopropyl)benzoate was placed in 30 mL of dichloromethane and 1.8 mL of pyridine. The solution was cooled to 0° C. and 1.2 mL of allyl chloroformate (dissolved in 5 mL of dichloromethane) was added dropwise at 0° C.-5° C. The mixture was left to react for 30 minutes at 0° C. and 2 hours at RT. The solution was combined with silica gel and evaporated down to the residue. This was chromatographed with dichloromethane on silica gel 70. Yield: 1.46 g of oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173699B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-1015be712b5b41f4981a9f14eea13522 |
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| Source note | uspto-grants-2012_05 |
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