HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913012Generated: November 1, 2026
Sodium borohydride → HCID 68015202, compound
https://huagongshe.com/reaction/1913012
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 68015073 | HCID 68015073 | — |
| Product | HCID 68015202 | HCID 68015202 | 99.5% |
Reaction Steps
(5-bromo-2-chloro-phenyl)-(4-ethoxy-3-fluoro-phenyl)methanone 4c (12.7 g, 35.5 mmol) was dissolved in 100 mL of mixed solution (THF and MeOH, v:v=1:1), followed by addition of sodium borohydride (2.68 g, 70 mmol) in batch in an ice bath. The reaction mixture was warmed and stirred for 30 minutes at room temperature. Thereafter, the reaction mixture was concentrated under reduced pressure after 15 mL acetone were added. The residue was dissolved in 150 mL ethyl acetate and washed with saturated sodium chloride solution (50 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-3-fluoro-phenyl)methanol 4d (12.7 g, orange 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-a1a438dbf26c4ecba98460307e7ad08d |
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| Source note | uspto-grants-2013_12 |
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