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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534947Generated: October 31, 2026

benzyl N-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}glycinate → N-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}glycine

https://huagongshe.com/reaction/534947

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl N-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}glycinateHCID 66751166—
CatalystPalladium hydroxideHCID 9942167—
SolventEthyl AcetateHCID 8857—
ProductN-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}glycineHCID 6675089198.2%

Reaction Steps

A suspension of benzyl N-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}glycinate (Example 86, 350 mg, 0.80 mmol) and palladium hydroxide (20% on carbon, wetted with ca. 50% water, 30 mg) in ethyl acetate (25 mL) was stirred under hydrogen atmosphere at room temperature for 3 h. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure to provide N-{[4-(2-tert-butylphenyl)piperazin-1-yl](oxo)acetyl}glycine (0.273 g, 98%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-5f3657dd611d49928b1ba766a8430216
Source noteuspto-grants-2014_10