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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226991Generated: November 4, 2026

Benzaldehyde → HCID 73554247, compound

https://huagongshe.com/reaction/2226991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium ChlorideHCID 5234—
ReactantSodium HydroxideHCID 14798—
ReactantL-Serine, methyl ester, hydrochloride (1:1)HCID 2723730—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductHCID 73554247HCID 73554247—

Reaction Conditions

Temperature4 °C

Reaction Steps

A solution of 20 g (0.129 mol) L-serine methyl ester hydrochloride (XXIV) in 100 mL MeOH was adjusted to pH 8 with 12.9 mL 10M NaOH thus precipitating NaCl. Benzaldehyde (15.0 g, 0.141 mol) was added and stirred well for 30 min. After cooling to 4° C., 2.43 g (0.064 mol) NaBH4 was added in parts over one hour. The reaction was then warmed to ambient temperature and stirred for another hour. Analysis by ion pair HPLC showed that aside from the desired product, identified by co-elution with material obtained by esterification of N-benzyl-L-serine, the only other product observed was benzyl alcohol. The reaction was filtered, concentrated, and dried. The thick residue was dissolved in 120 mL acetone, refiltered to remove more salt, adjusted to between pH 1 to 1.5 with HCL gas, 750 mL Et2O added, product collected by centrifugation, and dried, giving 28.1 g colorless hygroscopic solid. Chromatographic comparison to purified material showed this to contain 91.6 mmol (71%). MS (E.I., direct insertion) m/z(% relative abundance) 210(MH+)(5), 178(55), 150(64), 118(6), 106(29), 91(100); HRMS (+DCI, CH4) m/z calcd for C11H16NO3 (MH+) 210.113, found 210.112

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05350851
Source datasetuspto-grants-1994_09
ORD IDord-b764c863ddf24a7bb3f3ea017367d0e5
Source noteuspto-grants-1994_09