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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591074Generated: October 30, 2026

Acetyl chloride → 1-(3,4-dihydro-2H-1-benzopyran-6-yl)ethan-1-one

https://huagongshe.com/reaction/591074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantChromanHCID 136319—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product1-(3,4-dihydro-2H-1-benzopyran-6-yl)ethan-1-oneHCID 1235701899%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Aluminium chloride (1.19 g, 8.9 mmol) was added portionwise to a stirred solution of acetyl chloride (1.21 mL, 17.0 mmol) in dry dichloromethane (20 mL), previously cooled to −10° C., until homogeneous (5 min). The solution was added, via cannula, to a solution of 3,4-dihydro-2H-1-benzopyran (9a) (1.20 g, 8.9 mmol) in dry dichloromethane (17 mL) at −10° C. The mixture was stirred at the same temperature for 30 minutes before being poured into ice/concentrated hydrochloric acid (5:1, v/v, 126 mL). The stirring was maintained at room temperature for 2 hours and the solution was extracted with dichloromethane (3×50 mL). The organic layer was dried over sodium sulfate and concentrated in vacuo to provide 1-(3,4-dihydro-2H-1-benzopyran-6-yl)ethan-1-one (49a) (1.55 g, 8.8 mmol, 99%) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-4d852f4a432746b2936bff5bfc71437a
Source noteuspto-grants-2016_01