HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 178521639, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(Benzyloxy)cyclobutan-1-one | HCID 14932787 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178521639 | HCID 178521639 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06579875B1 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-fc9d55e2b23d4bcb80fa92cfeae946c7 |
| Source note | uspto-grants-2003_06 |