HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421213Generated: October 29, 2026
Potassium sodium tartarate → HCID 70296498, compound
https://huagongshe.com/reaction/1421213
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 53701259 | HCID 53701259 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 70296498 | HCID 70296498 | 76.4% |
Reaction Steps
A suspension of 1,1 g (3.0 mmoles) of 1-(2,4-dimethoxystyryl)-4-methyl-7,8-methylenedioxy-5H-2,3-benzodiazepine in 15 ml of anhydrous tetrahydrofurane is cooled to a temperature between 0° C. and 5° C., and 0.114 g (3.0 mmoles) of lithium aluminium hydride is added to it. The reaction mixture is stirred at 25° C. for 2 hours, cooled again to a temperature between 0° C. and 5° C. and decomposed with 0.36 ml of 10% aqueous potassium sodium tartrate solution. Then it is stirred further for 1 hour at 25° C., the precipitate is filtered off, the filtrate is dried and evaporated under reduced pressure. The crude end-product is recrystallized from 10 ml of ethanol, filtered, washed three times with 1 ml each of ethanol and dried at a temperature between 80° C. and 100° C. Thus 0.84 g (76.0%) of the desired product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06075018 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-bec79b617683465482d8a9204ac6c5a2 |
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| Source note | uspto-grants-2000_06 |
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