HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420300Generated: October 26, 2026
Hexane → (3,5-Difluoro-4-nitrophenyl)methanol
https://huagongshe.com/reaction/420300
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Dipotassium 2,3-dihydroxybutanedioate | HCID 6100505 | — |
| Reactant | Methyl 3,5-difluoro-4-nitrobenzoate | HCID 57386305 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3,5-Difluoro-4-nitrophenyl)methanol | HCID 55271003 | — |
Reaction Steps
To a solution of 3,5-difluoro-4-nitro-benzoic acid methyl ester (10.95 g, 50 mmol) in THF (250 mL) was added at 0-5° C. under argon a 1M DIBAL solution in hexane (165 mL, 165 mmol) within 1.5 h. The reaction mixture was stirred for 2.5 h at 0-5° C. before it was added to 200 mL cold 1M aq. potassium tartrate solution under ice-cooling. After stirring the reaction mixture for 0.5 h at 25° C. the aqueous phase was extracted with EtOAc. Combined organic extracts were washed with brine, dried over MgSO4, filtered and evaporated to provide the title compound as a yellow solid: TLC (hexane-EtOAc 1.1) Rf=0.35; HPLC RtA=1.31 min; 1H NMR (400 MHz, CDCl3): δ 7.12 (d, 2H), 4.77 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093406B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-65a054ff4d384189987d7ade0615bcaf |
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| Source note | uspto-grants-2012_01 |
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