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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040820Generated: November 2, 2026

(-)-Epichlorohydrin → HCID 86639883, compound

https://huagongshe.com/reaction/2040820

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(-)-EpichlorohydrinHCID 2734062—
ReactantHCID 136360510HCID 136360510—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
ProductHCID 86639883HCID 86639883—

Reaction Steps

To a solution of 2-ethyl-4-[5-(2-ethyl-6-methyl-pyridin-4-yl)-[1,2,4]oxadiazol-3-yl]-6-methyl-phenol (89 mg, 0.276 mmol) in 3 N aq. NaOH (1 mL) and isopropanol (4 mL), (R)-epichlorohydrine (142 mg, 1.53 mmol) is added. The mixture is stirred at rt for 24 h before another portion of (R)-epichlorohydrine (142 mg; 1.53 mmol) is added. Stirring is continued for another 24 h at rt. The mixture is diluted with EA (50 mL) and washed with 1M aq. NaOH (10 mL) and brine (10 mL). The org. phase is dried over MgSO4, filtered and evaporated to give crude (S)-2-ethyl-4-[3-(3-ethyl-5-methyl-4-oxiranylmethoxy-phenyl)-[1,2,4]oxadiazol-5-yl]-6-methyl-pyridine; LC-MS*: tR=1.11* min; [M+1]+=380.24.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580824B2
Source datasetuspto-grants-2013_11
ORD IDord-3e73b150dd32421ba60a6ce9b18dc3f8
Source noteuspto-grants-2013_11