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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048564Generated: October 30, 2026

Acetonitrile → HCID 58573156, compound

https://huagongshe.com/reaction/1048564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantBenzyl mercaptanHCID 7509—
ReactantHCID 58573730HCID 58573730—
ProductHCID 58573156HCID 58573156—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-1-((S)-1-cyclopropyl-2-hydroxyethyl)-3-methylpiperidin-2-one (1.35 g, 2.94 mmol; Example 252, Step A), benzyl mercaptan (0.691 ml, 5.89 mmol) and 2-(tributylphosphoranylidene) in acetonitrile (1.579 ml, 5.89 mmol) was heated to 100° C. for 2 h. The reaction mixture was cooled to RT, and extracted with 80 mL of EtOAc. The combined organics were washed with sat. aq. NH4Cl solution and brine, dried over Na2SO4, filtered and the filtrate was concentrated. The crude product was purified by chromatography on silica gel eluting with 0 to 50% EtOAc/hexane to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-638adfc9028e43b984916f8c91114244
Source noteuspto-grants-2013_10