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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1532449Generated: October 29, 2026

1,2-Dimethoxyethane → HCID 54094583, compound

https://huagongshe.com/reaction/1532449

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 15169699HCID 15169699—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54094583HCID 54094583100%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06201119B1
Source datasetuspto-grants-2001_03
ORD IDord-0d45eddd61584e92b944fa984f039748
Source noteuspto-grants-2001_03