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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618246Generated: October 29, 2026

3-Chloro-4-methyl-5-nitrobenzoic acid → (3-Chloro-4-methyl-5-nitrophenyl)methanol

https://huagongshe.com/reaction/618246

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-methyl-5-nitrobenzoic acidHCID 22107457—
SolventTetrahydrofuranHCID 8028—
Product(3-Chloro-4-methyl-5-nitrophenyl)methanolHCID 1878973849.9%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05952362
Source datasetuspto-grants-1999_09
ORD IDord-ee5e94817443458b8c55769922112184
Source noteuspto-grants-1999_09