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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21357Generated: October 30, 2026

Hydrochloric Acid → 2-(2-Acetoxypropyl)naphthalene

https://huagongshe.com/reaction/21357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantAcetic AnhydrideHCID 7918—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
Product2-(2-Acetoxypropyl)naphthaleneHCID 19933745—

Reaction Steps

In a four-necked flask equipped with a thermometer and stirrer, were placed 15.1 g (0.08 mole) of the compound (XII-1) obtained in Preparation Example 1, 50 ml of toluene and 20 ml of pyridine, thereafter 10.2 g (0.1 mole) of acetic anhydride and 0.1 g of 4-dimethylaminopyridine was added thereto, and the resulting mixture was stirred at 40°-50° C. for 4 hours. After completion of the reaction, the reaction mixture was poured into 50 ml of 4N hydrochloric acid to conduct extraction and layer separation. The organic layer obtained was washed successively with 1N hydrochloric acid, water, 5% aqueous sodium bicarbonate solution and water. The organic layer was then concentrated under reduced pressure to obtain 18.2 g of 2-(2-acetoxypropyl)naphthalene (XIII-1). Yield: 99 0%, nD20 1,5413

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05422038
Source datasetuspto-grants-1995_06
ORD IDord-12560695943c426e871f7f672340ce90
Source noteuspto-grants-1995_06