HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23605Generated: October 30, 2026
HCID 178455054, compound → HCID 178455052, compound
https://huagongshe.com/reaction/23605
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 178455054 | HCID 178455054 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178455052 | HCID 178455052 | 97.1% |
Reaction Steps
To a flask was added trans-N-benzyl-N-[4-(2,4-bis{[tert-butyl(dimethyl)silyl]oxy}phenyl) cyclohexyl]amine (500 mg, 0.95 mmol) and ethanol (20 ml). To the stirred solution was added palladium (10% w/w on activated carbon, 200 mg, 0.19 mmol) as a slurry in ethanol (5 ml). The reaction vessel was evacuated, then placed under hydrogen. The reaction mixture was stirred vigorously under an atmosphere of hydrogen for 18 hr, then filtered through a celite plug, washing with methanol (100 ml). The solvent was removed in vacuo affording the title compound (402 mg, 97%) as a colourless oil. δH(CDCl3) 0.01 (6H, s), 0.05 (6H, s), 0.78 (9H, s), 0.82 (9H, s), 1.08 (2H, m), 1.21 (2H, m), 1.62 (2H, m), 1.78 (2H, m), 2.59 (2H, m), 6.11 (1H, d), 6.22 (1H, dd), 6.78 (1H, d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06852747B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-808a09ddfc6d443cacb3f773193cb1c2 |
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| Source note | uspto-grants-2005_02 |
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