HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608335Generated: October 31, 2026
2-Chloroethanol → 2-Hydroxyethyl-3-benzyl-2-oxo-1,2,5,6,7,8-hexahydroquinoxaline
https://huagongshe.com/reaction/1608335
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Benzyl-5,6,7,8-tetrahydroquinoxalin-2(1H)-one | HCID 178517340 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-Hydroxyethyl-3-benzyl-2-oxo-1,2,5,6,7,8-hexahydroquinoxaline | HCID 14881353 | 96% |
Reaction Steps
Ethylene chlorohydrin (16.10 g, 0.2M) was added to a solution of 2-hydroxy-3-benzyl-5,6,7,8-tetrahydro quinoxaline (9.60 g, 40 mM) in dilute aqueous 5N NaOH (40 ml) and t-butanol (120 ml), and stirred at 60° C. for 3 hours. The t-butanol was distilled off in vacuo. The residue was extracted three times with chloroform, dried with anhydrous sodium sulfate and concentrated in vacuo. The residue was charged on a column of silica-gel (C-200, 220 g) packed with chloroform, and eluted with chloroform-methanol (200:1) to obtain compound 643 (10.90 g, yield: 83.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04870176 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-c9f2dc55ba1a4ac99b548fb0ae3115c1 |
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| Source note | uspto-grants-1989_09 |
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