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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369442Generated: October 27, 2026

Sodium borohydride → HCID 178521639, compound

https://huagongshe.com/reaction/1369442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(Benzyloxy)cyclobutan-1-oneHCID 14932787—
SolventEthanolHCID 702—
ProductHCID 178521639HCID 17852163992%

Reaction Steps

A mixture of 3-benzyloxycyclobutan-1-one (0.92 g, 5.22 mmol) (Ogura et al., Bull. Chem. Soc. Jpn., 1984, 57, 1637-1642) and sodium borohydride (0.20 g, 5.29 mmol) in ethanol (15 ml) was stirred at room temperature for 3.5 h. The mixture was filtered, washing with ethanol, and the filtrate was concentrated. Filtration through a plug of silica, eluting with ethyl acetate, gave cis-3-benzyloxy-1-hydroxycyclobutane (0.854 g, 92%) as a colourless oil; 1H NMR (250 MHz, CDCl3) δ1.75-2.00 (2H, m), 2.65-2.79 (2H, m), 3.62 (1H, qn, J=7 Hz), 3.90 (1H, broad qn, J=7 Hz), 4.41 (2H, s), 7.23-7.47 (5H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06579875B1
Source datasetuspto-grants-2003_06
ORD IDord-fc9d55e2b23d4bcb80fa92cfeae946c7
Source noteuspto-grants-2003_06