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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493484Generated: October 31, 2026

N-(t-butyldimethylsilyl)-4-(3-benzyloxycarbonyl-2-hydroxypropyl)-azetidin-2-one → N-(t-butyldimethylsilyl)-4-(3-carboxy-2-hydroxypropyl)-azetidin-2-one

https://huagongshe.com/reaction/1493484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(t-butyldimethylsilyl)-4-(3-benzyloxycarbonyl-2-hydroxypropyl)-azetidin-2-oneHCID 12804719—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-(t-butyldimethylsilyl)-4-(3-carboxy-2-hydroxypropyl)-azetidin-2-oneHCID 1513630892.9%

Reaction Steps

A mixture of crude N-(t-butyldimethylsilyl)-4-(3-benzyloxycarbonyl-2-Hydroxypropyl)-azetidin-2-one (13.46 g, 35.6 mmol), 10% palladium on charcoa, and ethanol (200 ml) is hydrogenated at 40 psi for 30 mins. The mixture is filtered and the filtrate is evaporated under vacuum and stripped with toluene to give N-(t-butyldimethylsilyl)-4-(3-carboxy-2-hydroxypropyl)-azetidin-2-one (9.51 g) as an off-white solid: IR (neat film from Me2CO) 3200 (br), 1735, and 1700 (shifts to 1590 with Et3N) cm-1 ; NMR (Me2CO-d6) 8 0.25 (s,6,2CH3), 0.98 (s,9,C(CH3)3) 1.17-2.33 (m,2,CH--C CH2 --CH), 2.50 (d,2,J=6.5, CH2CO2), 2.50-3.40 (m,2,H3 and H3β), 3.97 (m,2,H4 and CHOH); MS on bistrimethylsilyl derivative m/e 431 (M+), 416 (M+-57) and 332 (374-42).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05021566
Source datasetuspto-grants-1991_06
ORD IDord-05707bb103544f6bb8b0f15e5e52baf0
Source noteuspto-grants-1991_06