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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351515Generated: November 2, 2026

Hydrochloric Acid → Ethyl 2-chloro-3-[4-(2-methylchroman-2-ylmethoxy)phenyl]propionate

https://huagongshe.com/reaction/2351515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcrylateHCID 8821—
Reactant2-(4-Aminophenoxymethyl)-2-methylchromanHCID 15613913—
ReactantSodium NitriteHCID 23668193—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductEthyl 2-chloro-3-[4-(2-methylchroman-2-ylmethoxy)phenyl]propionateHCID 15613914—

Reaction Conditions

Temperature40 °C

Reaction Steps

0.7 ml of concentrated aqueous hydrochloric acid was dropped, whilst ice-cooling, into a solution of 500 mg of 2-(4-aminophenoxymethyl)-2-methylchroman (prepared as described in Preparation 4) in 5 ml of acetone, and then a solution of 170 mg of sodium nitrite in 2 ml of water was added dropwise to the resulting mixture. When the dropwise additon was complete, 2 ml of ethyl acrylate were added, and the reaction mixture was heated to 40° C. 10 mg of cuprous oxide were then added gradually, and the mixture was stirred for 30 minutes. At the end of this time, the acetone was distilled off under reduced pressure, and the residue was extracted with benzene. The benzene extract was dried over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure. The residue was subjected of silica gel column chromatography eluted with a 10:1 dy volume mixture of hexane and ethyl acetate, to afford 350 mg of the title compound as a pale yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873255
Source datasetuspto-grants-1989_10
ORD IDord-53991555ef984a70a798818fa1227b31
Source noteuspto-grants-1989_10