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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850152Generated: October 29, 2026

Water → (E)-methyl 2-[2-(6-chloropyrid-2-yloxymethyl)phenyl]-3-hydroxyacrylate

https://huagongshe.com/reaction/850152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl formateHCID 7865—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 2-(6-chloropyrid-2-yloxymethyl)phenylacetateHCID 10989960—
SolventTolueneHCID 1140—
Product(E)-methyl 2-[2-(6-chloropyrid-2-yloxymethyl)phenyl]-3-hydroxyacrylateHCID 1936633298.6%

Reaction Steps

Sodium methoxide (0.39 g, 6.9 mmol) and methyl formate (1 ml, 16 mmol) were added portionwise to a stirred solution of methyl 2-(6-chloropyrid-2-yloxymethyl)phenylacetate (1.0 g, 3.3 mmol) in dry toluene (15 ml) under a nitrogen atmosphere at room temperature. After 3 hours at room temperature the mixture was poured into water and extracted with ethyl acetate. The ethyl acetate extracts were washed with water, dried and the ethyl acetate removed to give (E)-methyl 2-[2-(6-chloropyrid-2-yloxymethyl)phenyl]-3-hydroxyacrylate (1.04 g, 95%) as a brown gum which was used in the final stage without further purification; 1H NMR(270 MHz)δ: 3.75(3H,s), 5.29(2H,s), 6.65(1H,d), 6,90(1H,d), 7.15-7.60(6H,m), 11.98(1H,d) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06015905
Source datasetuspto-grants-2000_01
ORD IDord-09ee9767a3e54b42a9fead86d62e5dd3
Source noteuspto-grants-2000_01