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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799894Generated: October 31, 2026

Ethyl 2-chloroacetoacetate → Chloro-(5-bromo-2-but-3-ynyloxyphenylhydrazono)acetic acid ethyl ester

https://huagongshe.com/reaction/1799894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-chloroacetoacetateHCID 11858—
ReactantSodium AcetateHCID 517045—
ReactantSodium NitriteHCID 23668193—
Reactant5-Bromo-2-but-3-ynyloxy-phenylamineHCID 58204909—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductChloro-(5-bromo-2-but-3-ynyloxyphenylhydrazono)acetic acid ethyl esterHCID 8665229895%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Chloro-3-oxo-butyric acid ethyl ester (1.94 g, 11.2 mmol) and sodium acetate (1.45 g, 17.8 mmol) were stirred in IMS (100 mL) to give a clear solution, then cooled to 0° C. Separately, 5-bromo-2-but-3-ynyloxy-phenylamine (2.68 g, 11.2 mmol) in 6M hydrochloric acid (6.8 mL) was cooled to 0° C. and a solution of sodium nitrite (0.77 g, 11.2 mmol) in water (11.2 mL) was added dropwise with stirring, keeping the temperature below 5° C. The aqueous acidic solution was added to the IMS solution, washed in with a little water, keeping the temperature below 5° C. After 1 h at 0-5° C., the mixture was diluted with water and extracted several times with ethyl acetate. The combined organic extracts were washed with water, dried (Na2SO4), filtered and concentrated in vacuo to give Chloro-(5-bromo-2-but-3-ynyloxyphenylhydrazono)acetic acid ethyl ester as a pale brown solid (3.96 g, 95%). LCMS: RT=4.97 min, [M+Na]+=395/397/399.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343955B2
Source datasetuspto-grants-2013_01
ORD IDord-5e8fbb71972c471faa8a930e8599e733
Source noteuspto-grants-2013_01