HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848864Generated: October 29, 2026
Methanol → 2-(4-Fluorophenoxy)acetaldehyde
https://huagongshe.com/reaction/848864
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Ethyl-p-fluorophenoxy acetate | HCID 88767291 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(4-Fluorophenoxy)acetaldehyde | HCID 11051869 | 45% |
Reaction Steps
To a stirred solution of 1.98 g (10 mmoles) of ethyl-p-fluorophenoxy acetate (Example 155) in 15 ml of dry toluene, cooled to -78° C., under argon, is added, dropwise over 30 minutes, 8 ml of a 1.4M solution of diisobutylaluminum hydride in toluene (11 mmoles). The mixture is stirred for 2 hours at -78° C., 1 ml of methanol is added, followed by 5 ml of water, dropwise. The gel formed is filtered through Celite and washed with 100 ml of ether, portionwise. The organic phase is separated, washed twice with 25 ml of a saturated brine solution, dried with magnesium sulfate, filtered, and evaporated. The oil obtained is distilled at 71°-73° C. (0.1 mm) to give 600 mg (45%) of the subject product as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04297516 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-a486dc1b85cf4efe86ec299946abe41f |
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| Source note | uspto-grants-1981_10 |
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