HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → α-(Bromomethyl)-5-thiazolemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Bromo-1-(1,3-thiazol-5-yl)ethan-1-one | HCID 19711315 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | α-(Bromomethyl)-5-thiazolemethanol | HCID 19711332 | 62.5% |
Reaction Steps
Sodium borohydride (38 mg, 1.0 mmol) was added in one portion to a solution of 207 mg (1.0 mmol) of the product from Example 3 in 2 mL of methanol at 0° C. After stirring for 0.75 h, water was added and the mixture extracted three times with diethyl ether. The combined organic phase was washed with brine, dried(MgSO4) and the solvent removed in vacuo. Flash chromatography (silica gel, 30-40% ethyl acetate-hexanes) afforded 130 mg (62%) of the title compound as a colorless oil: 1H NMR (400 MHz, CDCl3) δ8.78 (s, 1H), 7.83 (s, 1H), 5.28-5.24 (m, 1H), 3.70 (dd, 1H, J=10.6, 3.9 Hz), 3.61 (dd, 1H, J=10.6, 7.9 Hz), 2.95 (d, 1H, J=4.3 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705515 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-8862e28a38f84e3bb47d16712fc4e57d |
| Source note | uspto-grants-1998_01 |