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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231429Generated: October 27, 2026

Hydrochloric Acid → (2-Chloro-4-fluoro-5-nitrophenyl)methanol

https://huagongshe.com/reaction/231429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Chloro-4-fluoro-5-nitrobenzaldehydeHCID 13563775—
SolventTetrahydrofuranHCID 8028—
Product(2-Chloro-4-fluoro-5-nitrophenyl)methanolHCID 1362975270.7%

Reaction Steps

To a solution of 10.8 g (0.053 mole) of 2-chloro-4-fluoro-5-nitrobenzaldehyde in 100 ml of tetrahydrofuran was added 0.50 g (0.013 mole) of sodium borohydride portionwise. The reaction mixture was stirred for one hour after which dilute hydrochloric acid was added to destroy unreacted sodium borohydride. To this mixture was added 200 ml of methylene chloride, and the phases were separated. The organic phase was washed three times with water, dried over anhydrous magnesium sulfate, and filtered. The solvent was evaporated from the filtrate under reduced pressure, leaving a residue weighing 10.7 g. This residue was combined with 1.67 g of a similar residue another run of the same reaction. The combined residues were passed through a silica gel column, eluting with ethyl acetate/heptane (1/4) to yield 7.7 g of 2-chloro-4-fluoro-5-nitrobenzyl alcohol as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04846882
Source datasetuspto-grants-1989_07
ORD IDord-ef30e54f9f504dd79a79c8a1ed3a5323
Source noteuspto-grants-1989_07