HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5948Generated: October 26, 2026
Benzyl Alcohol → Benzyloxycarbonyl-3-methylenecyclobutanamine
https://huagongshe.com/reaction/5948
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Methylenecyclobutanecarboxylic acid | HCID 27475 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Benzyloxycarbonyl-3-methylenecyclobutanamine | HCID 86747233 | 68.5% |
Reaction Steps
To a stirred solution of 26.7 g (238 mmol) of 3-methylenecyclobutane carboxylic acid (Cripps, H. N.; Williams, J. K.; Sharkey, W. H. J. Am. Chem. Soc. 1959, 81, 2723-2728) in 100 mL of toluene at 0° C. was added 36.4 mL (262 mmol) of triethylamine and then 72.1 g (262 mmol) of diphenylphosphoryl azide. The reaction mixture was then heated at 80° C., and after 1 h, 28.33 g (262 mmol) of benzyl alcohol was added. After 15 h at 85° C., the cooled reaction mixture was poured into 1 L of ether, washed with saturated aqueous NaHCO3, and then saturated aqueous NaCl, dried over MgSO4, and then concentrated under reduced pressure. Chromatography of the residue in three portions on 1400 g of silica gel with 80:20/hexane:EtOAc afforded 35.4 g (63%) of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05246931 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-c0218d5b5bfa40d88a5132d0538e4b9e |
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| Source note | uspto-grants-1993_09 |
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