HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532449Generated: October 29, 2026
1,2-Dimethoxyethane → HCID 54094583, compound
https://huagongshe.com/reaction/1532449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 15169699 | HCID 15169699 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54094583 | HCID 54094583 | 100% |
Reaction Steps
To a cooled (0° C.) suspension of 8.53 parts of lithium aluminum hydride in 392 parts of 1,2dimethoxyethane there were added dropwise 20.19 parts of (S)-7-chloro-3,4-dihydro-3-methyl-1H-1,4-benzodiazepine-2,5-dione (prepared as intermediate 43) under argon. The mixture was left at room temperature for 3 hours and was then refluxed for 29 hours. After cooling to 0° C., there were added successively a mixture of 8.5 parts of water and 22.7 parts of tetrahydrofuran, 9.86 parts of NaOH (15%) and 25.5 parts of water. The whole was stirred for 24 hours and was then filtered. The precipitate was refluxed in 178 parts of tetrahydrofuran for 5 min and filtered off again. The combined filtrates were evaporated and the residual oil crystallized on standing, yielding 18.4 parts (100%) of (S)-7-chloro2,3,4,5-tetrahydro-3-methyl-1H-1,4-benzodiazepine (interm. 59).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06201119B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-0d45eddd61584e92b944fa984f039748 |
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| Source note | uspto-grants-2001_03 |
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