HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893225Generated: November 1, 2026
4-Phenylcyclohexanone → HCID 49763571, compound
https://huagongshe.com/reaction/1893225
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Phenylcyclohexanone | HCID 78605 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86646678 | HCID 86646678 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 49763571 | HCID 49763571 | — |
Reaction Steps
A solution of 4-phenyl-cyclohexanone (Aldrich, 1.5 g, 8.62 mmol) and N-(azetidin-3-ylcarbamoylmethyl)-3-trifluoromethyl-benzamide TFA salt (as prepared in the previous step, 3.89 g, 12.9 mmol) in DCM (20 mL) was treated with TEA (6 mL, 43 mmol) for 10 min followed by NaBH(OAc)3 (Aldrich, 3.65 g, 17.2 mmol) for another 4 hours at room temperature. The reaction was quenched with saturated sodium bicarbonate. The organic layer was separated and the aqueous layer was extracted 3 times with a chloroform/IPA “cocktail” (˜3:1, v/v). The combined organic layers were dried over anhydrous Na2SO4, filtered and concentrated to give the crude product, which was then purified by a CombiFlash® system using ethyl acetate and 7N NH3 in MeOH as eluent (from pure ethyl acetate to 5% 7N NH3 in MeOH in ethyl acetate) to afford the two title compounds as white solids.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513229B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-b33e184be415416ab32c3477acd29bee |
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| Source note | uspto-grants-2013_08 |
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