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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-boranyl-2-methylpropan-2-amine | HCID 3639180 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 6-Benzyl-3b,4,5,6,7,7a-hexahydro-1-thia-6-aza-cyclopenta[alpha]inden-8-one | HCID 59789429 | — |
| Reactant | HCID 178419134 | HCID 178419134 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Benzyl-4,5,6,7,7a,8-hexahydro-3bH-1-thia-6-aza-cyclopenta[alpha]indene | HCID 131727038 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423056B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-e6dcc8a7a840485494b9e868fe1ebc7d |
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| Source note | uspto-grants-2008_09 |
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