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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473236Generated: October 30, 2026

Methanol → Methyl 3-fluoromethyl-5-hydroxymethylbenzoate

https://huagongshe.com/reaction/473236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantDimethyl 5-fluoromethylisophthalateHCID 67254949—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-fluoromethyl-5-hydroxymethylbenzoateHCID 6725356780%

Reaction Steps

Dimethyl 5-fluoromethylisophthalate (33) (3.16 g, 14.0 mmol) was dissolved in THF (10.5 mL). The air was evacuated from the reaction system, and then Ar was charged therein. To the solution were added NaBH4 (638 mg, 16.9 mmol), and then a mixted solution of THF:MeOH (8.8 mL:2.6 mL) slowly dropwise. The reaction mixture was refluxed for 1 hour. TLC was used to confirm the progress of the reaction. Then, the reaction was quenched with HCl (1 N, 14 mL). The mixture was extracted with EtOAc. The organic layer was washed with a saturated sodium chloride aqueous solution, dried over anhydrous sodium sulfate, and evaporated under reduced pressure. The residue was purified by neutral silica gel column chromatography (hexane:EtOAc=5:1 to 2:1) to isolate methyl 3-fluoromethyl-5-hydroxymethylbenzoate (34) (2.21 g, 80%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633304B2
Source datasetuspto-grants-2014_01
ORD IDord-18cebb2628424d1c93711dd52da84bce
Source noteuspto-grants-2014_01