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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473234Generated: November 1, 2026

Methanol → Dimethyl 5-(hydroxymethyl)isophthalate

https://huagongshe.com/reaction/473234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTrimethyl benzene-1,3,5-tricarboxylateHCID 75881—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
ProductDimethyl 5-(hydroxymethyl)isophthalateHCID 1390732461.2%

Reaction Steps

Trimethyl 1,3,5-benzenetricarboxylate (5.02 g, 19.9 mmol) was dissolved in THF (15 mL). The air was evacuated from the reaction system, and then Ar was charged therein. To the solution were added NaBH4 (901 mg, 23.8 mmol), and then a mixed solution of THF:MeOH (12.5 mL:3.7 mL) slowly dropwise. The reaction mixture was refluxed for 30 minutes. TLC was used to confirm the progress of the reaction. Then, the reaction was quenched with HCl (1 N, 20 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 to remove the solvent. The residue was purified by neutral silica gel column chromatography (hexane:EtOAc=4:1 to 3:1) to isolate dimethyl 5-hydroxymethylisophthalate (32) (2.73 g, 61%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633304B2
Source datasetuspto-grants-2014_01
ORD IDord-022365251f784f2ea9a07cd7e9ff0fca
Source noteuspto-grants-2014_01