HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343647Generated: November 1, 2026
Sodium Bicarbonate → HCID 54172520, compound
https://huagongshe.com/reaction/343647
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 22941573 | HCID 22941573 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 54172520 | HCID 54172520 | 59.1% |
Reaction Steps
4.2 g of N-(-N-methyl-2(R)-tert-butoxycarbonylamino-3-(triphenylmethylthio)propionyl)-N,O-dimethylhydroxylamine in 15 cm3 of diethyl ether are added, at a temperature in the region of -45° C., to a suspension of 0.386 g of lithium aluminium hydride in 35 cm3 of diethyl ether. The temperature is allowed, with stirring, to rise to approximately 0° C. After cooling to a temperature in the region of -35° C., a solution of 1.77 g of sodium hydrogen carbonate in 6.5 cm3 of water is added. The organic phase is washed 3 times with 10 cm3 of a normal hydrochloric acid solution, then twice with 10 cm3 of a saturated sodium hydrogen carbonate solution and finally with 10 cm3 of a saturated sodium chloride solution. The organic phase is dried over magnesium sulphate, filtered and concentrated under reduced pressure. 2.2 g of N-methyl-N-tert-butoxycarbonyl-S-(triphenylmethyl)cysteinal are obtained, which are used in the following stage without other purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05861529 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-4a668b992abe4b40b84214a2c162d47c |
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| Source note | uspto-grants-1999_01 |
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