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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462874Generated: October 31, 2026

Triethylamine → 1-t-Butyldimethylsilyl-4-tritylthio-2-azetidinone

https://huagongshe.com/reaction/1462874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant4-Tritylthio-2-azetidinoneHCID 12780164—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product1-t-Butyldimethylsilyl-4-tritylthio-2-azetidinoneHCID 1292874593.3%

Reaction Steps

Triethylamine (1.62 ml, 11.6 mmoles) was added dropwise in 5 min to a cooled (0°) and stirred solution of 4-tritylthio-2-azetidinone (3.5 g, 10.1 mmoles) and chloro-t-butyldimethylsilane (1.68 g, 12.7 mmoles) in DMF (35 ml). The reaction mixture was stirred at room temperature for 18 h, diluted with water (250 ml) and ether (200 ml). The organic phase was washed with water (3×50 ml), dried and concentrated to leave an oil (4.33 g). Crystallization from pentane gave a total of 4.1 g (89%) of the title compound as a white solid, m.p. 113°-4°. δ(ppm, CDCl3): 7.45 (15H, m, aromatics), 4.2 (1H, dd, H-4), 2.63 (1H, dd, J=4, J=16, H-3), 2.13 (1H, dd, J=2, J=16, H-3), 1.0 (9H, s t-Bu), 0.35 (6H, s, Me).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04461727
Source datasetuspto-grants-1984_07
ORD IDord-45d436463cd346288c6513b4f43837f6
Source noteuspto-grants-1984_07