HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266360Generated: October 31, 2026
Trimethyl borate → (4-Chloro-2,5-difluorophenyl)methanol
https://huagongshe.com/reaction/1266360
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Chloro-2,5-difluorobenzoic acid | HCID 2733274 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Product | (4-Chloro-2,5-difluorophenyl)methanol | HCID 18550157 | 100.5% |
Reaction Steps
To a mixture of 4-chloro-2,5-difluoro-benzoic acid (15 g, 78 mmol) tetrahydrofuran (THF) (75 mL) and trimethylborate (26 mL, 230 mmol) was added borane-methylsulfide complex (86 mL, 86 mmol, 10 M solution in DMS), and the mixture was stirred for 18 hours at ambient temperature. Additional borane-methylsulfide complex (2.47 mL, 24.7 mmol) was added to drive the reaction to completion. The mixture was poured into 1M aqueous NaOH, extracted 3× with ether, and the combined organic layers were dried over anhydrous MgSO4, filtered and concentrated in vacuo. Trituration of the solid residue with ether-hexane afforded 14 g of (4-chloro-2,5-difluoro-phenyl)-methanol as a colorless solid. 1H NMR (400 MHz, CDCl3) δ 7.26 (dd, 1H, J=6, 8.8 Hz), 7.11 (dd, 1H, J=6, 9.2 Hz), 4.71 (d, 2H, J=6.0 Hz), 1.80 (t, 1H, J=6.0 Hz) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06548526B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-94fc84c34ed44cdcaae0ac9aac5835b4 |
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| Source note | uspto-grants-2003_04 |
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