HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201805Generated: October 25, 2026
Methanol → Methyl 2,6-dichloro-4-(hydroxymethyl)benzoate
https://huagongshe.com/reaction/2201805
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Dimethyl 2,6-dichloroterephthalate | HCID 7730227 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2,6-dichloro-4-(hydroxymethyl)benzoate | HCID 66712920 | 80% |
Reaction Steps
A solution of dimethyl 2,6-dichlorobenzene-1,4-dicarboxylate (2.3 g, 8.7 mmol) in tetrahydrofuran (10 mL) was treated with sodium borohydride (0.496 g, 13 mmol) and heated to refluxing temperature. The reaction mixture was then treated drop wise with methanol (1 mL) and continued refluxing for about 2 hours. The reaction mixture was warmed to room temperature and quenched with saturated aqueous ammonium chloride solution followed by partitioning with ethyl acetate. The combined organic layer was washed with brine, dried over sodium sulfate, filtered and concentrated. The crude product was purified by silica gel column chromatography using ethyl acetate in hexane (10%) as an eluant to yield methyl 2,6-dichloro-4-(hydroxymethyl)benzoate as a colorless liquid (1.6 g, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09364466B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-0a80337fcf494295834c2681c507fd2a |
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| Source note | uspto-grants-2016_06 |
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