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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6735Generated: October 27, 2026

Acetone → 2-Methoxy-8,9-dihydro-5H-benzo[7]annulen-6(7H)-one

https://huagongshe.com/reaction/6735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2,6,6-trimethoxy-6,7,8,9-tetrahydro-5H-benzocyclohepteneHCID 12353829—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product2-Methoxy-8,9-dihydro-5H-benzo[7]annulen-6(7H)-oneHCID 1236917780.2%

Reaction Steps

A solution of 2,6,6-trimethoxy-6,7,8,9-tetrahydro-5H-benzocycloheptene (387 mg) and p-toluenesulfonic acid monohydrate (31 mg) was stirred in 5 mL of 1:1 water:acetone. The mixture was diluted with 50 mL of dichloromethane and 50 mL of saturated sodium hydrogen carbonate. The aqueous layer was re-extracted with 50 mL more dichloromethane and the combined organics were dried over sodium sulfate. Evaporation of the solvent gave 250 mg of 2-methoxy-5,7,8,9-tetrahydro-benzocyclohepten-6-one, which was converted to 2-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-ylamine by using Procedure X.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084154B2
Source datasetuspto-grants-2006_08
ORD IDord-443e59999fd64eac976cc8d305d90497
Source noteuspto-grants-2006_08