HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299660Generated: November 1, 2026
Sodium Bicarbonate → (2S)-1-[N-benzyl-N-(3-isopropoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl)-amino]-3-phenoxy-2-propanol
https://huagongshe.com/reaction/2299660
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (2S)-2-(phenoxymethyl)oxirane | HCID 1534345 | — |
| Reactant | Ytterbium triflate | HCID 2733225 | — |
| Reactant | N-benzyl-(3-isopropoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl)amine | HCID 18007411 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2S)-1-[N-benzyl-N-(3-isopropoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl)-amino]-3-phenoxy-2-propanol | HCID 57196896 | 79.1% |
Reaction Steps
Under nitrogen, to a solution of N-benzyl-(3-isopropoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl)amine (258 mg) and (2S)-3-phenoxy-1,2-epoxypropane (138 mg) in dichloromethane (5 ml) was added ytterbium(III) trifluoromethanesulfonate (52 mg) at room temperature, and the mixture was stirred at the same temperature for 60 hours. The resulting mixture was poured into saturated aqueous sodium hydrogencarbonate and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=10:1 to 5:1) to give (2S)-1-[N-benzyl-N-(3-isopropoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-yl)-amino]-3-phenoxy-2-propanol (303 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06495546B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-be4ed5a1968345a9a472f54853cdd027 |
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| Source note | uspto-grants-2002_12 |
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