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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744906Generated: October 31, 2026

Propionyl chloride → HCID 22226102, compound

https://huagongshe.com/reaction/1744906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionyl chlorideHCID 62324—
Reactant6-Ethoxy-1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthaleneHCID 226705—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductHCID 22226102HCID 22226102—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019034B2
Source datasetuspto-grants-2006_03
ORD IDord-70db157907e0418d8ef64e5f8bf885ff
Source noteuspto-grants-2006_03