HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473234Generated: November 1, 2026
Methanol → Dimethyl 5-(hydroxymethyl)isophthalate
https://huagongshe.com/reaction/473234
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Trimethyl benzene-1,3,5-tricarboxylate | HCID 75881 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl 5-(hydroxymethyl)isophthalate | HCID 13907324 | 61.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08633304B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-022365251f784f2ea9a07cd7e9ff0fca |
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| Source note | uspto-grants-2014_01 |
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