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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1459114Generated: November 3, 2026

Benzaldehyde → HCID 22885226, compound

https://huagongshe.com/reaction/1459114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantL-Tyrosine 1,1-dimethylethyl esterHCID 6950582—
SolventMethanolHCID 887—
ProductHCID 22885226HCID 22885226—

Reaction Steps

16.9 g (71.5 mmol) of tyrosine-tert-butyl ester and 8.33 g (78.6 mmol) of benzaldehyde are stirred in 50 ml of methanol for 3 hours at 24° C. and then mixed with 3.37 g (53.6 mmol) of sodium cyanoborohydride. After 24 hours of stirring at room temperature, the batch is adjusted to pH 2 by careful addition of semiconcentrated hydrochloric acid, then neutralized with concentrated aqueous sodium bicarbonate solution and after substantial evaporation of methanol with ethyl acetate, it is shaken out. The organic phase is dried on anhydrous magnesium sulfate, filtered and concentrated by evaporation. The residue is chromatographed on silica gel with diethyl ether/hexane/triethylamine; the product-containing fractions are combined and concentrated by evaporation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05853699
Source datasetuspto-grants-1998_12
ORD IDord-2d6bc6a2a57f40e684852199caa493e9
Source noteuspto-grants-1998_12