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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 260615Generated: October 26, 2026

Acetyl chloride → 1-Acetoxy-2-methylnaphthalene

https://huagongshe.com/reaction/260615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant2-Methyl-1-naphtholHCID 24055—
SolventEthyl AcetateHCID 8857—
Product1-Acetoxy-2-methylnaphthaleneHCID 1180572763.1%

Reaction Steps

A solution of 9.48 g (60 mmole) of 2-methyl-1-naphthol and 8.10 g (80 mmole) of triethylamine in 50 mL of ethyl acetate was cooled to below 5° C. in an ice-bath. 5.50 g (70 mmole) of acetyl chloride was added at a rate such that the temperature did not rise about 5° C. The reaction mixture was stirred for an additional one hour, diluted with 50 mL of ethyl acetate, and washed with water then brine. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated to give an oily residue. Crystallization in hexane yielded 7.58 g (63% yield) of the title compound with a melting point of 81°-83° C. and an 1HNMR as follows: (300 MHz, DMSO-d6) δ 2.26 ) (s, 3H), 2.48 (s, 3H), 7.42 (d, 1H, J=9 Hz), 7.46-7.55 (m, 2H), 7.47-7.81 (m, 2H), 7.92 (d, 1H, J=9 Hz). The mass spectrum showed a molecular ion at m/z 200.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05529583
Source datasetuspto-grants-1996_06
ORD IDord-78e6d1cf38c14d24b7bae736936f3e0d
Source noteuspto-grants-1996_06