HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628384Generated: October 29, 2026
Dimethyl 5-chloroisophthalate → Methyl 3-chloro-5-(hydroxymethyl)benzoate
https://huagongshe.com/reaction/628384
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl 5-chloroisophthalate | HCID 224975 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-chloro-5-(hydroxymethyl)benzoate | HCID 53712641 | — |
Reaction Steps
To a solution of dimethyl 5-chloroisophthalate (10.0 g, 43.7 mmol, Astatech) in methanol (50 mL) and methylene chloride (50 mL) at 0° C. was added sodium borohydride (5.5 g, 140 mmol, Aldrich). The reaction was allowed to gradually reach room temperature and stir for 1 hour. Additional portions of sodium borohydride (0.50 g, 13 mmol) were added at 2 hours and 3 hours. The reaction mixture was cooled to 0° C. and the reaction was quenched with water. The layers were separated and the aqueous layer was extracted with three portions of DCM. The combined organic extracts were dried over sodium sulfate, filtered and concentrated. The product was purified by flash chromatography, eluting with a gradient from 0-25% EtOAc in hexanes. Yield: (4.51 g, 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309246B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-12d76dd990a44861a9635243cd8208f8 |
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| Source note | uspto-grants-2016_04 |
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