HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629757Generated: October 31, 2026
4-Hydroxybenzaldehyde → 4-(4,4,4-Trifluorobutoxy)benzaldehyde
https://huagongshe.com/reaction/1629757
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4,4,4-Trifluorobutan-1-ol | HCID 136307 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4,4,4-Trifluorobutoxy)benzaldehyde | HCID 53724788 | 71% |
Reaction Steps
To a solution of 4-hydroxybenzaldehyde (20 g, 164 mmol) and 4,4,4-trifluorobutan-1-ol (25 g, 195 mmol) in anhydrous CH2Cl2 (500 mL) at 0° C. under Ar was added a solution of PPh3 (51.5 g, 196 mmol) in CH2Cl2 (200 mL) over 15 min, and then DIAD (36.4 g, 180 mmol) in anhydrous CH2Cl2 (150 mL) was added dropwise. The mixture was stirred at 0° C. for 0.5 h. The reaction was warmed to rt and stirred for another 3 h. The solvent was removed in vacuo and the residue was triturated with CH2Cl2 three times to remove insoluble solids. The combined CH2Cl2 washings were concentrated and the residue was purified by silica gel chromatography (330 g silica gel, eluted with EtOAc in hexanes) to provide Intermediate 2A (27 g, 71%) as a light brown oil. LCMS Anal. Calc'd for C11H11F3O2 232.20, found [M+H] 233.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791091B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-4253b1626534403ba673b7dd1a275090 |
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| Source note | uspto-grants-2014_07 |
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