HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84306Generated: October 29, 2026
Sodium borohydride → HCID 178521561, compound
https://huagongshe.com/reaction/84306
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-[(4-Bromo-phenoxy)-difluoro-methyl]-cyclohexanone | HCID 67250266 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178521561 | HCID 178521561 | — |
Reaction Steps
To a stirred solution of 4-[(4-bromo-phenoxy)-difluoro-methyl]-cyclohexanone (1050 mg, 3.290 mmoles) in ethanol (16.4 mL, 0.2M) was added NaBH4 (249 mg, 6.58 mmoles) 0° C. The solution was stirred at 0° C. for 20 minutes and then warmed to room temperature for 20 minutes. The reaction was quenched with 1 N HCl to a pH of ˜7, and extracted three times with ethyl acetate. The organics where combined, dried over magnesium sulfate, filtered and concentrated. Cis/trans isomers were then separated by chiral purification. Isolated 260 mg of trans isomer (24%). 1H NMR (400 MHz, METHANOL-d4) δ ppm 1.39 (s, 2 H) 1.51-1.65 (m, 2 H) 1.83-1.96 (m, 2 H) 2.01-2.21 (m, 2 H) 2.38-2.47 (m, 1 H) 7.03-7.14 (m, 2 H) 7.41-7.58 (m, 2 H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846933B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-fa629faf936e40789d6699c9df645c77 |
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| Source note | uspto-grants-2014_09 |
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