HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106754Generated: October 30, 2026
3-Chloro-4-methyl-5-nitrobenzoic acid → (3-Chloro-4-methyl-5-nitrophenyl)methanol
https://huagongshe.com/reaction/1106754
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-4-methyl-5-nitrobenzoic acid | HCID 22107457 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Chloro-4-methyl-5-nitrophenyl)methanol | HCID 18789738 | 49.9% |
Reaction Steps
4.2 g of 3-chloro-4-methyl-5-nitro benzoic acid was dissolved in 20 ml dry THF and the solution was cooled to 0° C. BH3 -THF (28 ml) solution was added in 2 ml portions. After 1 hr, the reaction mixture was poured onto 100 g of ice containing saturated NaHCO3 solution. The mixture was extracted with ether (3×75 ml). The extracts were washed with brine, dried (anhydrous MgSO4), filtered, and concentrated. The resultant brown oil was applied to a SiO2 column as a solution in toluene and eluted with 25% ethyl acetate in hexane to give 1.96 g of (3-chloro-4-methyl-5-nitrophenyl)methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057349 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-99401c4c6d1f4eb9a08b8f5eafe278c8 |
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| Source note | uspto-grants-2000_05 |
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