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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724912Generated: October 30, 2026

Water → α-(Bromomethyl)-5-thiazolemethanol

https://huagongshe.com/reaction/724912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Bromo-1-(1,3-thiazol-5-yl)ethan-1-oneHCID 19711315—
SolventMethanolHCID 887—
Productα-(Bromomethyl)-5-thiazolemethanolHCID 1971133262.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05705515
Source datasetuspto-grants-1998_01
ORD IDord-8862e28a38f84e3bb47d16712fc4e57d
Source noteuspto-grants-1998_01