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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973267Generated: October 31, 2026

1-Iodo-3-methylbutane → HCID 21402622, compound

https://huagongshe.com/reaction/973267

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Iodo-3-methylbutaneHCID 10924—
Reactantethyl 5-hydroxy-4-oxo-4H-chromene-2-carboxylateHCID 2801504—
ReactantThalliumHCID 5359464—
SolventChloroformHCID 6212—
ProductHCID 21402622HCID 21402622—

Reaction Conditions

Temperature100 °C

Reaction Steps

A stirred mixture of 21.67 parts of ethyl 5-hydroxy-4-oxo-4H-1-benzopyran-2-carboxylate, thallium salt and 99 parts of 1-iodo-3-methylbutane was refluxed for one hour. After cooling, chloroform was added to the reaction mixture and the insoluble thallium salts were removed by filtration. The chloroform filtrate was washed with cold N sodium hydroxide solution, then washed with water and the volatile components were removed by evaporation. Sodiumbicarbonte soluton was added to the oily residue obtained and the mixture was stirred at 100° C for 2 hours. After cooling, the solution ws extracted with chloroform and the aqueous layer was separated. This aqueous extract was acidified with 2H hydrochloric acid and the solid which precipitated was collected by filtration, washed with water and dried to give 6.16 parts of 5-(3-methyl-n-butoxy)-4-oxo-4H-1-benzopyran-2-carboxylic acid, m.p. 181°-183° C (after crystallistion from ethyl acetate/light petroleum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04055654
Source datasetuspto-grants-1977_10
ORD IDord-a692ffbb1cbd455a95eb28441e465954
Source noteuspto-grants-1977_10