HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628909Generated: October 26, 2026
Thionyl Chloride → (5-Methoxy-2-nitrophenyl)methanol
https://huagongshe.com/reaction/628909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Methoxy-2-nitrobenzoic acid | HCID 339209 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Methoxy-2-nitrophenyl)methanol | HCID 53405061 | 66% |
Reaction Steps
To a solution of 5-methoxy-2-nitrobenzoic acid (20.0 g, 0.102 mol) in anhydrous THF (200 mL) was added SOCl2 (20 mL), the mixture was refluxed for 4 hours. The solvent was removed under reduced pressure and the residue was dissolved in anhydrous THF (100 mL). The solution was added dropwise to a suspension of NaBH4 (7.70 g, 0.202 mol) in anhydrous THF (100 mL) and DMF (140 mL) at 0° C. over a period of 30 minutes. The mixture was stirred at 30° C. for 3 hours, then quenched with ice-water (100 mL) and basified by 2M NaOH to pH 8. An EtOAc workup was followed by removal of solvent in vacuo and purification by column chromatography (PE/EtOAc=1/1) to give the product (12.0 g, yield 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315462B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-c67d59cf94584228b325a7a6d9c68531 |
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| Source note | uspto-grants-2016_04 |
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