HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913000Generated: November 3, 2026
Potassium borohydride → HCID 86685117, compound
https://huagongshe.com/reaction/1913000
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium borohydride | HCID 4192641 | — |
| Reactant | HCID 86685116 | HCID 86685116 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 86685117 | HCID 86685117 | 99.5% |
Reaction Steps
(5-bromo-2-chloro-phenyl)-(4-ethoxy-2,3-difluoro-phenyl)methanone 3c (8.0 g, 21.3 mmol) was dissolved in 240 mL of mixed solution (THF and MeOH, v:v=1:1), followed by addition of potassium borohydride (1.73 g, 32.0 mmol) in an ice bath. The reaction mixture was stirred for 16 hours at room temperature. Thereafter, 50 mL 1 M hydrochloric acid were added. The reaction mixture was concentrated under reduced pressure and extracted with dichloromethane (100 mL×2). The organic extract was combined, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure to obtain the title compound (5-bromo-2-chloro-phenyl)-(4-ethoxy-2,3-difluoro-phenyl)methanol 3d (8.0 g, yellow grease), which was used directly in the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609622B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-78511bc3fbdc4720a70ab414bc62934e |
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| Source note | uspto-grants-2013_12 |
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