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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037358Generated: November 1, 2026

alpha-Chlorohydrin, (+)- → HCID 68628850, compound

https://huagongshe.com/reaction/2037358

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-Chlorohydrin, (+)-HCID 148904—
ReactantHCID 136344049HCID 136344049—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventSodium HydroxideHCID 14798—
ProductHCID 68628850HCID 6862885032.4%

Reaction Steps

To a solution of 2-ethyl-4-[5-(4-isobutyl-6-methyl-pyridin-2-yl)-[1,2,4]oxadiazol-3-yl]-6-methyl-phenol (41 mg, 0.116 mmol) in isopropanol (3 mL) and 3 N aq. NaOH (0.4 mL), (S)-3-chloro-1,2-propanediol (66 mg, 0.577 mmol) is added. The mixture is stirred at 65° C. for 16 h before another portion of (S)-3-chloro-1,2-propanediol (66 mg, 0.577 mmol) and 3 N aq. NaOH (0.4 mL) is added. Stirring is continued at 65° C. for 24 h. The mixture is cooled to rt, diluted with water, and repeatedly extracted with diethyl ether. The combined org. extracts are dried over MgSO4, filtered and concentrated. The crude product is purified on prep. TLC using DCM:methanol 9:1 to give the title compound (16 mg) as a colourless oil; LC-MS: tR=1.02 min, [M+H]+=426.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575200B2
Source datasetuspto-grants-2013_11
ORD IDord-2dd74b0199bf4e3fbdc27bc1e0d47b7f
Source noteuspto-grants-2013_11