HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040648Generated: October 31, 2026
Benzyl Alcohol → Benzyl (3-oxocyclobutyl)carbamate
https://huagongshe.com/reaction/2040648
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 3-Oxocyclobutane-1-carboxylic acid | HCID 4913358 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Benzyl (3-oxocyclobutyl)carbamate | HCID 19794323 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580762B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-bbf2f5c9d9b24d9a8079896f04c76be3 |
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| Source note | uspto-grants-2013_11 |
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