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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444374Generated: October 30, 2026

Ethyl bromoacetate → HCID 22814861, compound

https://huagongshe.com/reaction/444374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
Reactanttrans-1,2-CyclohexanediolHCID 92886—
ReactantSodiumHCID 5360545—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 22814861HCID 2281486169.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a slurry of 54 grams of 55% sodium hydride in 1000 mls of toluene is portionwise added 140 grams of trans-1,2-cyclohexanediol at 90° C. with concommitant release of hydrogen. The resulting mass, containing the monosodium salt of trans-1,2-cyclohexanediol is stirred at 100° C. for 30 minutes. Ethyl bromoacetate (203 grams) is added dropwise to the stirred reaction mass at 100° C. over a 30 minute period. After stirring for 30 minutes, the mass is cooled to 20° C. Water (100 ml) is added and the organic layer is distilled to afford 130 grams of trans-hexahydro-1,4-benzodioxan-2-one. The product is purified by distillation through a 1"×12" Goodloe® packed column to afford a semi solid (m.p. 20°-22° C., bp. 97° C. at 1.2 mm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04264456
Source datasetuspto-grants-1981_04
ORD IDord-7ece4b82c18145c983d5bcf66ee1da95
Source noteuspto-grants-1981_04