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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261446Generated: November 3, 2026

Epichlorohydrin → HCID 86622508, compound

https://huagongshe.com/reaction/2261446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantHCID 59593547HCID 59593547—
SolventAcetic AcidHCID 176—
SolventIsopropanolHCID 3776—
SolventSodium HydroxideHCID 14798—
ProductHCID 86622508HCID 8662250832.7%

Reaction Steps

A solution of 3-(4-hydroxy-3-methyl-phenyl)-1-((1aS,5aR)-1,1,2-trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalen-4-yl)-propan-1-one (179 mg, 0.525 mmol, Intermediate 4) in isopropanol (10 mL) and 3 N aq. NaOH (4 mL) is treated with epichlorohydrine (197 mg, 1.58 mmol). The reaction mixture is stirred at 70 for 1.5 h. The mixture is diluted with acetic acid (0.3 mL) and the solvent is removed under reduced pressure. The residue is purified by prep. HPLC (Waters Xterra MS18, 75×30 mm ID, 10 μm, 10 to 95% acetonitrile in water containing 0.5% formic acid) to give 3-(3-methyl-4-oxiranylmethoxy-phenyl)-1-((1aS,5aR)1,1,2-trimethyl-1,1a,5,5a-tetrahydro-3-thia-cyclopropa[a]pentalen-4-yl)-propan-1-one (68 mg) as a pale brown oil; LC-MS: tR=1.15 min, [M+1]+=397.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846964B2
Source datasetuspto-grants-2010_12
ORD IDord-c5cffb7092de4a32812a2364013d3872
Source noteuspto-grants-2010_12