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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343647Generated: November 1, 2026

Sodium Bicarbonate → HCID 54172520, compound

https://huagongshe.com/reaction/343647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 22941573HCID 22941573—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 54172520HCID 5417252059.1%

Reaction Conditions

Temperature-35 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861529
Source datasetuspto-grants-1999_01
ORD IDord-4a668b992abe4b40b84214a2c162d47c
Source noteuspto-grants-1999_01