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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443783Generated: October 29, 2026

Octanoic acid, 2-acetyl-8-(2-chloro-4-methoxyphenoxy)-, ethyl ester → HCID 178492574, compound

https://huagongshe.com/reaction/443783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOctanoic acid, 2-acetyl-8-(2-chloro-4-methoxyphenoxy)-, ethyl esterHCID 514183—
ReactantThiosemicarbazideHCID 2723789—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductHCID 178492574HCID 17849257455.2%

Reaction Steps

A mixture of 11.1 g (0.03 m) of ethyl 2-acetyl-8-(2-chloro-4-methoxyphenoxy)octanoate, 2.73 g (0.03 m) of thiosemicarbazide and 1.62 g (0.03 m) of sodium methoxide in 15 ml of methanol was heated at reflux for 24 hours. The solid product was collected, washed with 50% aqueous ethanol and recrystallized from ethanol to give 5.6 g of 4-[6-(2-chloro-4-methoxyphenoxy)-hexyl]-5-methyl-1H-pyrazol-3-ol, m.p. 145°-146° C.; MIC=6 microg/ml (herpes 2). (During this reaction the thiocarbamyl group (CSNH2) of the thiosemicarbazide was cleaved so that the reaction product is the same as that obtained when unsubstituted hydrazine is used.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04261928
Source datasetuspto-grants-1981_04
ORD IDord-99b98dc226cd441d944bcb9b09a21f7d
Source noteuspto-grants-1981_04