HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015696Generated: October 31, 2026
Lithium borohydride → (5-Chloro-2-(methylsulfonyl)phenyl)methanol
https://huagongshe.com/reaction/1015696
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Methyl 5-chloro-2-(methylsulfonyl)benzoate | HCID 66877882 | — |
| Solvent | 2-(Oxolan-2-yl)ethan-1-ol | HCID 11989572 | — |
| Product | (5-Chloro-2-(methylsulfonyl)phenyl)methanol | HCID 66885987 | 89.3% |
Reaction Steps
(Step 2) To a solution of methyl 5-chloro-2-(methylsulfonyl)benzoate obtained in Step 1 (2.65 g) in tetrahydrofuran-ethanol (50 ml+5 ml) was added lithium borohydride (348 mg) at 0° C. The mixture was stirred at 60° C. for 2 hr, treated with ice, and extracted with ethyl acetate. The extract was washed successively with 1N hydrochloric acid and saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=2:1) to give [5-chloro-2-(methylsulfonyl)phenyl]methanol (2.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985862B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-90ddb0e3b8184d4b967e30e80fe09290 |
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| Source note | uspto-grants-2011_07 |
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