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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048350Generated: November 2, 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/1048350

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 numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-4c7d1fad85c043cbb4a032e8babf5154
Source noteuspto-grants-2013_10