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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065915Generated: November 3, 2026

alpha-Chlorohydrin, (+)- → HCID 59392504, compound

https://huagongshe.com/reaction/2065915

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Chlorohydrin, (+)-HCID 148904—
ReactantHCID 136170273HCID 136170273—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
ProductHCID 59392504HCID 5939250411.5%

Reaction Steps

To a solution of 4-[5-(5,6-diethyl-pyridin-3-yl)-[1,2,4]oxadiazol-3-yl]-2-ethyl-6-methyl-phenol (100 mg, 0.296 mmol) in isopropanol (10 mL) and 3 N aq. NaOH (3 mL), (S)-3-chloro-1,2-propanediol (98 mg, 0.89 mmol) is added. The mixture is stirred at 60° C. for 24 h before another portion of (S)-3-chloro-1,2-propanediol (98 mg, 0.89 mmol) is added. Stirring is continued at 60° C. for 2 days. The mixture is diluted with EA and washed with sat. aq. NaHCO3 solution. The org. extract is dried over MgSO4, filtered and evaporated. The crude product is purified by chromatography on prep. TLC plates with EA-heptane to give (S)-3-{4-[5-(5,6-diethyl-pyridin-3-yl)-[1,2,4]oxadiazol-3-yl]-2-ethyl-6-methyl-phenoxy}-propane-1,2-diol (14 mg) as a red oil; LC-MS: tR=0.93 min, [M+1]+=412.16.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288554B2
Source datasetuspto-grants-2012_10
ORD IDord-be66c2f7874947428716cb5b866a8d1e
Source noteuspto-grants-2012_10