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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5948Generated: October 26, 2026

Benzyl Alcohol → Benzyloxycarbonyl-3-methylenecyclobutanamine

https://huagongshe.com/reaction/5948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
Reactant3-Methylenecyclobutanecarboxylic acidHCID 27475—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductBenzyloxycarbonyl-3-methylenecyclobutanamineHCID 8674723368.5%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05246931
Source datasetuspto-grants-1993_09
ORD IDord-c0218d5b5bfa40d88a5132d0538e4b9e
Source noteuspto-grants-1993_09