HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423262Generated: October 31, 2026
Sodium borohydride → 2-Chloro-1-(6-fluorochroman-2-yl)ethanol
https://huagongshe.com/reaction/2423262
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-chloro-1-(6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanone | HCID 16755387 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-1-(6-fluorochroman-2-yl)ethanol | HCID 67243124 | 70% |
Reaction Steps
A solution under stirring of 2-chloro-1-(6-fluoro-3,4-dihydro-2H-chromen-2-yl)ethanone (0.33 g, 1.28 mmol, 88.4 A %) in ethanol (2.5 ml) was cooled to 0° C. under nitrogen. NaBH4 (60.1 mg, 1.59 mmol) was added to the solution and the reaction mixture stirred for 2 hours. After checking that the starting product had disappeared by GC, the mixture was diluted with demi water (7 ml) and dichloromethane (7 ml) and the phases separated. The organic stratum was dried under anhydrous sodium sulphate, filtered and concentrated under vacuum to give raw 2-chloro-1-(6-fluoro-3,4-dihydro-2H-chromen-2-yl) ethanol as a mixture of diastereoisomers 54:46 (0.30 g, 70% yield, 67.9 A %).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07960572B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-63c947e7ab5145d2ab3af2f0f34bffe0 |
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| Source note | uspto-grants-2011_06 |
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