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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783909Generated: October 30, 2026

Acetic Acid → HCID 66735236, compound

https://huagongshe.com/reaction/1783909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl CarbonateHCID 12021—
ReactantSodium hydrideHCID 24758—
Reactant6-Chloro-2-tetraloneHCID 4456139—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 66735236HCID 6673523663.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

10.1 g (252 mmol) of 60% sodium hydride in oil, 621 ml of toluene and 14.18 ml (163 mmol) of dimethyl carbonate are introduced into a 2 l reactor. The reaction mixture is stirred at reflux for 1 h. A solution of 15.2 g (84 mmol) of 6-chloro-3,4-dihydro-1H-naphthalen-2-one in 268 ml of toluene is subsequently added. The reaction mixture is heated at reflux for 24 h. The reaction mixture is subsequently cooled to 0° C. and then acidified by addition of 92 ml of acetic acid. 114 ml of water are added and the separated organic phase is separated by settling and washed with three times 150 ml of water and then with 100 ml of a saturated aqueous sodium chloride solution. The organic phase is subsequently dried over magnesium sulphate and then concentrated under reduced pressure. The residue is purified by chromatography on a silica column (elution being carried out with a mixture of cyclohexane and of dichloromethane) to result in 12.8 g (53.6 mmol) of the expected product used as is in the following stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501449B2
Source datasetuspto-grants-2009_03
ORD IDord-36ae9e63c57349b388155145f013119f
Source noteuspto-grants-2009_03