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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709249Generated: October 29, 2026

Hydrochloric Acid → HCID 14835692, compound

https://huagongshe.com/reaction/1709249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 14835691HCID 14835691—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
ProductHCID 14835692HCID 14835692—

Reaction Steps

4.67 g of ethyl (E)-3-(3-amino-4-isopropylphenyl)acrylate was dissolved in 46.7 ml of acetic acid. To the solution was added 46.7 ml of 2N hydrochloric acid with ice-cooling. To the mixture was dropwise added 10 ml of an aqueous solution containing 1.52 g of sodium nitrite. The mixture was stirred for 30 minutes at the same temperature. The reaction mixture was added to 30 ml of 6N hydrochloric acid solution containing 2.18 g of cuprous chloride, with ice-cooling. The mixture was stirred for 1 hour at the same temperature and then for 2 hours at room temperature. To the reaction mixture was added 100 ml of ethyl acetate. The organic layer was separated and washed with water. Thereto was added 50 ml of water. The mixture was adjusted to about pH 7 with sodium hydrogencarbonate. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue was purified by a column chromatography (eluant: n-hexane/ethyl acetate=20/1) to obtain 3.57 g of colorless oily ethyl (E)-3-(3-chloro-4-isopropylphenyl)acrylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04948796
Source datasetuspto-grants-1990_08
ORD IDord-2b923bc737234e6b93247b22e82d6786
Source noteuspto-grants-1990_08