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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040648Generated: October 31, 2026

Benzyl Alcohol → Benzyl (3-oxocyclobutyl)carbamate

https://huagongshe.com/reaction/2040648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantDiisopropylethylamineHCID 81531—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant3-Oxocyclobutane-1-carboxylic acidHCID 4913358—
SolventTolueneHCID 1140—
ProductBenzyl (3-oxocyclobutyl)carbamateHCID 1979432350%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 3-oxocyclobutanecarboxylic acid (1.0 g, 8.77 mmol) and DIEA (1.92 g, 14.92 mmol) in toluene (8 mL) was added DPPA (2.89 g, 10.52 mmol) at rt. The mixture was heated to 60° C. under Argon for 3 h, then benzyl alcohol (1.14 g, 10.52 mmol) was added. The mixture was stirred at 60° C. overnight. The reaction was concentrated, the residue was purified by SGC (PE:EA=8:1) to afford the desired compound (240 mg, yield 50%). 1H NMR (500 MHz, CDCl3): δH, 7.38-7.33 (m, 5H), 5.12 (d, J=7.5 Hz, 2H), 4.34-4.33 (brs, 1 H), 3.44-3.39 (m, 2H), 3.10-3.07 (brs, 2H) ppm; ESI-MS (m/z): 220.2 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580762B2
Source datasetuspto-grants-2013_11
ORD IDord-bbf2f5c9d9b24d9a8079896f04c76be3
Source noteuspto-grants-2013_11