HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744906Generated: October 31, 2026
Propionyl chloride → HCID 22226102, compound
https://huagongshe.com/reaction/1744906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | 6-Ethoxy-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene | HCID 226705 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22226102 | HCID 22226102 | — |
Reaction Steps
Propionyl chloride (1.44 mL, 16.6 mmol) was added to a stirring solution of 3-ethoxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene (Intermediate 2, 3.5 g, 15.1 mmol) in dichloromethane (100 mL), and the solution was cooled to 0° C. Aluminum trichloride (2.21 g, 16.6 mmol) was added over two to three minutes, the ice-bath was removed, the yellow solution was stirred for 1 h at room temperature. The solution was poured over ice in a separatory funnel, and the products were extracted three times with ether. The combined organic layers were washed with 10% aqueous sodium hydroxide, brine and dried over magnesium sulfate. The solvent was removed in vacuo to give the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07019034B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-70db157907e0418d8ef64e5f8bf885ff |
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| Source note | uspto-grants-2006_03 |
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