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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606103Generated: October 30, 2026

1-Bromo-3-methylbutane → HCID 21545978, compound

https://huagongshe.com/reaction/1606103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-methylbutaneHCID 7891—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 23336681HCID 23336681—
SolventAcetoneHCID 180—
ProductHCID 21545978HCID 21545978—

Reaction Steps

A mixture of 9 parts of ethyl 6-hydroxy-1-thiachromone-2-carboxylate, 15 parts of isoamyl bromide and 14 parts of anhydrous potassium carbonate in 130 parts of acetone was stirred and heated under reflux for 18 hours. Insoluble material was then filtered off and washed with acetone and the total acetone solution was evaporated to leave a yellow solid, which was crystallized from ethanol to give 4.1 parts of ethyl 6-(3-methylbutoxy)-1-thiachromone-2-carboxylate, melting point 83°-84°C. This entire product was heated under reflux for 2 hours with a solution of 1.5 parts of sodium bicarbonate in 35 parts of water and 25 parts of methanol. The methanol was then boiled off and the solution was diluted with 70 parts of water. The aqueous solution was thoroughly washed with ether, filtered then acidified with concentrated hydrochloric acid. A precipitate was obtained which was filtered off, washed with water and dried, then extracted with boiling benzene. The product was then filtered off and dried to leave 3.95 parts of 6-(3-methylbutoxy)-1-thiachromone-2-carboxylic acid, melting point 208°-209°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952013
Source datasetuspto-grants-1976_04
ORD IDord-6e0924ff196c4f82b73cd0521f37f515
Source noteuspto-grants-1976_04