HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 962838Generated: October 30, 2026
Acetyl chloride → 1-(3-Fluoro-4-methoxyphenyl)ethan-1-one
https://huagongshe.com/reaction/962838
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2-Fluoroanisole | HCID 67576 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-(3-Fluoro-4-methoxyphenyl)ethan-1-one | HCID 96828 | — |
Reaction Steps
Aluminum chloride (80.0 g, 0.6 mol) and chloroform (750 mL) were placed in a 2 L three-necked round bottom flask fitted with a mechanical stirrer and cooled by means of an ice bath. To the stirred solution was added acetyl chloride (51.0 g, 0.65 mol) dropwise, maintaining the temperature between 5°-10° C. The mixture was allowed to stir for 10 minutes at 5° C. before the dropwise addition at 5°-10° C. of 2-fluoroanisole (63.06 g, 0.5 mol. The mixture was stirred at 0°-10° C. for 1 hour and poured into ice (1 L). The resultant layers were separated and the aqueous layer was extracted with methylene chloride (2×250 mL). The combined organic layers were washed with water (2×150 mL), dried over magnesium sulfate, and concentrated to 300 mL. Hexanes crystallized from the mixture: mp 92°-94° C.; 1H NMR (d6 -DMSO) 7.8 (m, 2H), 7.3 (t, J=8.7Hz, 1H), 3.9 (s, 3H), 2.5 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05760068 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-9e4ff675f7d5409d96f062fc9845f864 |
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| Source note | uspto-grants-1998_06 |
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