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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129602Generated: October 30, 2026

Hydrochloric Acid → (E)-methyl 2-[2-(3-chlorosulphonylphenoxy)phenyl]-3-methoxypropenoate

https://huagongshe.com/reaction/129602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
Reactant(E)-methyl 2-[2-(3-aminophenoxy)phenyl]-3-methoxypropenoateHCID 15125769—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product(E)-methyl 2-[2-(3-chlorosulphonylphenoxy)phenyl]-3-methoxypropenoateHCID 15125770—

Reaction Steps

A solution of (E)-methyl 2-[2-(3-aminophenoxy)phenyl]-3-methoxypropenoate (0.4 g) in glacial acetic acid (2 ml) was treated with 5.8M hydrochloric acid (1 ml), at -10° C. The stirred solution was then treated with sodium nitrite (0.1 g in 2 ml of water) still at -10° C. After 30 minutes, the resulting solution (containing the diazonium salt) was added to a stirred mixture of glacial acetic acid (0.5 ml) saturated with sulphur dioxide, containing 0.1 g of cuprous chloride (effervescence). After 30 minutes, the reaction mixture was poured into water and extracted with ether. The ether extracts were neutralized with a saturated aqueous solution of sodium bicarbonate, dried and concentrated to give (E)-methyl 2-[2-(3-chlorosulphonylphenoxy)phenyl]-3-methoxypropenoate (0.14 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468857
Source datasetuspto-grants-1995_11
ORD IDord-4fbefb3eb8c44357970fe6534025c7c1
Source noteuspto-grants-1995_11