HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421272Generated: October 30, 2026
Methyl Ethyl Ketone → HCID 178505532, compound
https://huagongshe.com/reaction/2421272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 178511760 | HCID 178511760 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178505532 | HCID 178505532 | 12% |
Reaction Steps
A mixture containing (S)-cyclohexyl[4-(4-fluorophenyl)-1H-imidazol-2-yl]methanamine (prepared in Stage 5.2; 519 mg; 0.0015 mol), triethylamine (0.4 ml; 0.003 mol) and butanone (140 mg; 0.002 mol) in 10 ml of methanol is stirred for thirty minutes at 23° C. Sodium triacetoxyborohydride (630 mg; 0.003 mol) is then added. The reaction mixture is stirred for sixteen hours then poured into water. After extraction with ethyl acetate, the organic phase is washed with a saturated solution of sodium chloride then dried over magnesium sulphate. The solvent is evaporated off and the residue is purified on a silica column (eluent: CH2Cl2-MeOH mixture/95-05). A white-coloured powder is obtained with a yield of 12%. Melting point: 170-172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07956075B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-9407549af8cd4ba9bbe05091973d5f14 |
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| Source note | uspto-grants-2011_06 |
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