Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840022Generated: October 30, 2026

Hydrochloric Acid → HCID 53674838, compound

https://huagongshe.com/reaction/840022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDichloromethaneHCID 6344—
Reactant2-Chloro-N,N-diethyl-1,1,2-trifluoroethan-1-amineHCID 136184—
ReactantHCID 54467524HCID 54467524—
SolventWaterHCID 962—
ProductHCID 53674838HCID 53674838—
ProductHCID 86733917HCID 86733917—

Reaction Steps

A mixture of 25 g. of methyl 6-methoxy1-hydroxy-1,2,3,4-tetrahydro-2-naphthylacetate, 38 g. of 1-diethylamino-1,1,2trifluoro-2-chloroethane and 150 ml. of methylene chloride are allowed to stand for 24 hours. The fluorination reaction mixture is added to 250 ml. of water containing 12 g. of hydrogen chloride; the resulting mixture is separated and the methylene chloride phase is washed with water, dried over sodium sulfate, and evaporated to yield methyl 6-methoxy-1-fluoro-1,2,3,4-tetrahydro-2-naphthylacetate and 6-methoxy-1,2-dihydro-2-naphthylacetate. The mixture is separated on alumina eluting with acetone: diethyl ether (1:4) and the separated fractions are identified by ultraviolet spectroscopy. The fraction containing methyl 6-methoxy-1-fluoro-2-naphthylacetate is evaporated and the residue is refluxed with 23 g. of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone and 500 ml. of xylene for six hours. The cooled mixture is filtered and chromatographed on alumina eluting with chloroform. The fraction containing the product is evaporated to yield methyl 6-methoxy-1-fluoro- 2-naphthylacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04097674
Source datasetuspto-grants-1978_06
ORD IDord-41dcc91e2e454170935841be1f761e11
Source noteuspto-grants-1978_06