HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128155Generated: October 29, 2026
Ethyl bromoacetate → HCID 22814861, compound
https://huagongshe.com/reaction/128155
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | trans-1,2-Cyclohexanediol | HCID 92886 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22814861 | HCID 22814861 | 69.1% |
Reaction Steps
To a slurry of 54 grams of 55% sodium hydride in 1,000 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04259214 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-9d8f76816d1845a993a3def94dfb9834 |
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| Source note | uspto-grants-1981_03 |
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