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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449236Generated: November 1, 2026

Hydrochloric Acid → HCID 20350647, compound

https://huagongshe.com/reaction/1449236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantDichloromethaneHCID 6344—
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantHCID 54175266HCID 54175266—
ProductHCID 13023173HCID 1302317314%
ProductHCID 20350647HCID 2035064781%

Reaction Conditions

Temperature80 °C

Reaction Steps

In 26 ml of 1,2-dimethoxyethane, 1.2 g (0.0026 mole) of 1-[N-benzyl-o-(2,6-dichloroanilino)phenyl]-2-methylsulfinyl-2-methylthioethylene was dissolved and then, 13 ml of conc. HCl was added and the mixture was stirred at 80° C. for 4 hours. The reaction mixture was cooled and 80 ml of methylene chloride and 10 ml of water were added to extract the reaction product and the separated water phase was further mixed with 70 ml of methylene chloride to extract the reaction product. Both of methylene chloride phases were combined, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue was separated by a column chromatography (silica gel: Wako gel Q-23 manufactured by Wako Junyaku and developing solvent:n-hexane:acetone=2:1) to obtain 0.14 g (yield: 14%) of N-benzyl-o-(2,6-dichloroanilino)phenyl acetic acid and 0.88 g (yield: 81%) of methyl N-benzyl-o-(2,6-dichloroanilino)phenylthioacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04189595
Source datasetuspto-grants-1980_02
ORD IDord-ddffbd3595b24f63825b6be4d2dae32e
Source noteuspto-grants-1980_02