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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777281Generated: November 1, 2026

Acetaldehyde → HCID 86670461, compound

https://huagongshe.com/reaction/1777281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantWaterHCID 962—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86670460HCID 86670460—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86670461HCID 8667046138%

Reaction Steps

150 μl (2.4 mmol) of acetaldehyde are added to 369 mg (1.5 mmol) of methyl (S)-3-tert-butoxycarbonylamino-2-ethylaminopropanoate in 5 ml of tetrahydrofuran then stirred for 30 minutes at ambient temperature. After cooling to 0° C., 189 mg (3 mmol) of sodium cyanoborohydride are added and the reaction medium is stirred at ambient temperature for 36 h. Water is added and the medium is extracted with ethyl acetate. The organic phase is washed with water, dried over magnesium sulphate, filtered then concentrated. The crude residue obtained is purified by chromatography over silica gel eluted with a 70/30 heptane/ethyl acetate mixture. 150 mg (38%) of methyl (S)-3-tert-butoxycarbonylamino-2-diethylaminopropanoate are obtained in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266848B2
Source datasetuspto-grants-2016_02
ORD IDord-c5c95652c89d441b8124b081b2c335fe
Source noteuspto-grants-2016_02