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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55522Generated: October 29, 2026

Tetrahydrofuran → Ethyl 2-amino-3-t-butyldimethylsilyloxy-3-(2-chloropyridin-3-yl)propionate

https://huagongshe.com/reaction/55522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriphenylphosphineHCID 11776—
ReactantEthyl 2-azido-3-t-butyldimethylsilyloxy-3-(2-chloropyridin-3-yl)propionateHCID 23298343—
SolventWaterHCID 962—
ProductEthyl 2-amino-3-t-butyldimethylsilyloxy-3-(2-chloropyridin-3-yl)propionateHCID 23298326113%

Reaction Steps

A mixture of 5.6 g of ethyl 2-azido-3-t-butyldimethylsilyloxy-3-(2-chloropyridin-3-yl)propionate (prepared described in Preparation 77), 7.5 g of triphenylphosphine and 18 ml of a 8:1 by volume mixture of tetrahydrofuran and water was stirred at room temperature for 3 hours. At the end of this time, the reaction mixture was freed from the solvent by distillation. The residue was purified by column chromatography through silica gel, using a 5:1 by volume mixture of hexane and ethyl acetate and subsequently a 50:1 by volume mixture of methylene chloride and methanol as the eluent, to give 5.9 g of the title compound having Rf=0.59 (on silica gel thin layer chromatography using a 15:1 by volume mixture of methylene chloride and methanol as the developing solvent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05624935
Source datasetuspto-grants-1997_04
ORD IDord-df8c882a0a654b42aa2c255e5ff3a760
Source noteuspto-grants-1997_04