HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586612Generated: November 1, 2026
Acetyl chloride → 1-(4-(Methylthio)phenyl)ethan-1-one
https://huagongshe.com/reaction/586612
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Thioanisole | HCID 7520 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 1-(4-(Methylthio)phenyl)ethan-1-one | HCID 74501 | — |
Reaction Steps
Acetyl chloride (8.2 g, 0.105 mol) is added to a suspension of AlCl3 (16 g, 0.12 mol) in dichloroethane (50 ml) cooled to 0° C.; the mixture is stirred for 15 min and a solution of thioanisole (12.4 g, 0.1 mol) in dichloroethane (20 ml) is then added dropwise; the temperature is kept below 20° C. by cooling (30 min). The mixture is stirred for a further 1 h and allowed to stand at RT overnight. The Lewis acid complex is decomposed by addition of ice water (100 ml) with cooling, the organic phase is separated in a separating funnel, and the aqueous phase is extracted a further 2 times with dichloroethane (100 ml). The combined extracts are dried over Na2SO4 sicc. and concentrated to ¼ of the starting volume. The red-brown residue (15.2 g) is washed with diethyl ether (20 ml) and hexane (20 ml): 12 g of light red (brick-red) substance result.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936632B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-81864a8930494914b6d7ebd096764e73 |
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| Source note | uspto-grants-2005_08 |
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