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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30268Generated: October 30, 2026

Hydrochloric Acid → 6-Benzyl-4,5,6,7,7a,8-hexahydro-3bH-1-thia-6-aza-cyclopenta[alpha]indene

https://huagongshe.com/reaction/30268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantN-boranyl-2-methylpropan-2-amineHCID 3639180—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant6-Benzyl-3b,4,5,6,7,7a-hexahydro-1-thia-6-aza-cyclopenta[alpha]inden-8-oneHCID 59789429—
ReactantHCID 178419134HCID 178419134—
SolventDichloromethaneHCID 6344—
Product6-Benzyl-4,5,6,7,7a,8-hexahydro-3bH-1-thia-6-aza-cyclopenta[alpha]indeneHCID 13172703873%

Reaction Steps

A slurry of AlCl3 (571 mg, 4.29 mmol) in CH2Cl2 (4 ml) was treated with tert-butylaminoborane (746 mg, 8.58 mmol) at 0° C. and stirred for 30 minutes. Next, a solution of the product from step f) (406 mg, 1.43 mmol) in CH2Cl2 (3 ml) was added dropwise to the AlCl3/borane solution. After 2 hours at 0° C., the crude reaction mixture was poured into cold 10% HCl, treated with 2 M NaOH to pH 12 and extracted with CH2Cl2 (3×75 ml). The combined organic extracts were washed with brine (75 ml) and dried (MgSO4). The solvent was evaporated in vacuo and the crude product was purified by silica-gel chromatography using a ethyl acetate/hexanes gradient (0% to 75% ethyl acetate) to give 279 mg (73%) of the subtitle compound. MS calculated for C17H19NS+H 270, observed 270.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423056B2
Source datasetuspto-grants-2008_09
ORD IDord-e6dcc8a7a840485494b9e868fe1ebc7d
Source noteuspto-grants-2008_09