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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6395Generated: October 30, 2026

Methanol → 1-Carbomethoxy-6-chloro-3,4-dihydronaphthalene

https://huagongshe.com/reaction/6395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
Reactant6-Chloro-3,4-dihydronaphthalene-1-carbonitrileHCID 19793278—
SolventSulfuric AcidHCID 1118—
Product1-Carbomethoxy-6-chloro-3,4-dihydronaphthaleneHCID 1979317126%

Reaction Steps

6-Chloro-1-cyano-3,4-dihydronaphthalene (5 g, 263 mmol), lit ref, was dissolved in 77% sulfuric acid in methanol and the resulting solution was heated at 95°-100° C. for 2.5 h. The reaction mixture was allowed to cool to ambient temperature and 45 mL was added, followed by 5 mL of water. The reaction mixture was stirred at ambient temperature for 2 days and then concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water. The organic layer was concentrated in vacuo. The residue was purified by chromatography on silica gel eluted with 20% ethyl acetate in hexane to give 1.53 g (26% yield) of the title compound; MS DCl--NH3M/Z: 240 (M+H)+ ; 1H NMR (CDCl3) δ2.37-2.45 (2H, m), 2.75 (2H, t, J=7.5 Hz), 3.85 (3H, s), 7.15 (1H, d, J=1.5 Hz), 7.15 (1H, d, 9 Hz), 7.2 (1H, d, J=7.5 Hz), 7.77 (1H, d, J=7.5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05248677
Source datasetuspto-grants-1993_09
ORD IDord-0e9e6791f66b44a5853ffa9b8e1fcd15
Source noteuspto-grants-1993_09