HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397829Generated: October 29, 2026
Sodium Bisulfate → 2-Chloro-3-(trifluoromethyl)benzyl alcohol
https://huagongshe.com/reaction/397829
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | 2-Chloro-3-(trifluoromethyl)benzaldehyde | HCID 2736672 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-3-(trifluoromethyl)benzyl alcohol | HCID 2778108 | 92.9% |
Reaction Steps
Sodium borohydride (2.54 g, 67.1 mmol) was added to a solution of 2-chloro-3-(trifluoromethyl)benzaldehyde (purchased at Interchim, cat. # 21117, 10.0 g, 47.9 mmol) in a mixture of DCM (40 ml) and 2-propanol (20 ml), while the mixture was cooled with a water bath. The reaction mixture was stirred for 16 hours at room temperature. At 0° C., a 10% aqueous solution of sodium hydrogensulphate (20 ml) was added dropwise. The reaction mixture was diluted with DCM (100 ml) and water (100 ml). The phases were separated. The organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate (100 ml) and dried over magnesium sulphate. The solvent was removed in vacuo to give 9.37 g of crude (2-chloro-3-(trifluoromethyl)phenyl)methanol, which was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610721B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-3eca8dfac2d24514a271c24ebfa8e05f |
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| Source note | uspto-grants-2003_08 |
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