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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366640Generated: October 25, 2026

(Phenylmethoxy)acetaldehyde → phenylmethyl (2S)-2-methyl-4-{2-[(phenylmethyl)oxy]ethyl}-1-piperazinecarboxylate

https://huagongshe.com/reaction/1366640

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Phenylmethoxy)acetaldehydeHCID 108989—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantBenzyl (2S)-2-methylpiperazine-1-carboxylateHCID 40425199—
SolventDichloromethaneHCID 6344—
Productphenylmethyl (2S)-2-methyl-4-{2-[(phenylmethyl)oxy]ethyl}-1-piperazinecarboxylateHCID 6693599958%

Reaction Steps

A solution of phenylmethyl (2S)-2-methyl-1-piperazinecarboxylate (commercially available) (1 g, 4.3 mmol) and benzyloxyacetaldehyde (0.9 mL, 6.4 mmol) in DCM (50 mL) was stirred for 30 minutes, and then NaBH(OAc)3 (1.36 g, 6.4 mmol) was added. The reaction was stirred overnight before being quenched with 1 M NaOH. The phases were separated and the aqueous layer was extracted with DCM. The combined organics were washed with brine, dried over sodium sulfate and concentrated to a crude residue, which was purified by silica gel chromatography (5-95% EtOAc in hexane) yielding phenylmethyl (2S)-2-methyl-4-{2-[(phenylmethyl)oxy]ethyl}-1-piperazinecarboxylate (0.93 g, 58%). LCMS: (M+H)+: 369.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893056B2
Source datasetuspto-grants-2011_02
ORD IDord-ba015d2a15f246e69cfccaecc06d6998
Source noteuspto-grants-2011_02