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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 932039Generated: October 29, 2026

(3S,4R)-4-(3-chlorophenyl)-3-(4-chlorophenyl)-3,4-dihydro-2H-1,2-thiazin → (3S,4R)-4-(3-chlorophenyl)-3-(4-chlorophenyl)-1,2-thiazinan

https://huagongshe.com/reaction/932039

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3S,4R)-4-(3-chlorophenyl)-3-(4-chlorophenyl)-3,4-dihydro-2H-1,2-thiazinHCID 67999141—
Catalyst(1,5-Cyclooctadiene)pyridine(tricyclohexylphosphine)iridium hexafluorophosphateHCID 5702647—
SolventDichloromethaneHCID 6344—
Product(3S,4R)-4-(3-chlorophenyl)-3-(4-chlorophenyl)-1,2-thiazinanHCID 68000201—

Reaction Steps

A solution of 4.14 g (11.69 mmol) of (3S,4R)-4-(3-chlorophenyl)-3-(4-chlorophenyl)-3,4-dihydro-2H-1,2-thiazin (Example 117, Step B) in dichloromethane (63.0 mL) was purged with argon three times, and then Crabtree's catalyst (835.2 mg, 1.027 mmol) was added to the reaction mixture. The reaction was purged again with argon, and then a hydrogen atmosphere was placed over the reaction. The solution was stirred at ambient temperature for 15 hours, at which point the reaction was concentrated down to an oil. Purification by flash chromatography on silica gel (0 to 4% MeOH in DCM gradient) provided the title compound as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296736B2
Source datasetuspto-grants-2016_03
ORD IDord-d8611dab00ef46b29bf93e2d003d1f79
Source noteuspto-grants-2016_03