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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970511Generated: October 30, 2026

Triphenylphosphine → (S)-4-(4-Benzyl-2H-tetrazol-5-yl)-2-tert-butoxycarbonylamino-butyric acid benzyl ester

https://huagongshe.com/reaction/1970511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantAzidotrimethylsilaneHCID 78378—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant(S)-4-Benzylcarbamoyl-2-tert-butoxycarbonylamino-butyric acid benzyl esterHCID 15674275—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product(S)-4-(4-Benzyl-2H-tetrazol-5-yl)-2-tert-butoxycarbonylamino-butyric acid benzyl esterHCID 66854446—

Reaction Steps

To a suspension of 0.83 g (S)-4-benzylcarbamoyl-2-tert-butoxycarbonylamino-butyric acid benzyl ester and 1.28 g triphenylphosphine in 16 ml acetonitrile were added dropwise at 0° C. 1.00 ml diisopropylazodicarboxylate and after 2 minutes 0.67 ml trimethylsilylazide over a period of 10 minutes. After 30 minutes the mixture was allowed to warm to RT and stirred for 12 h. The mixture was cooled to 0° C. and 0.67 ml aqueous sodium nitrite (2.9 M) were added, after 30 minutes a solution of 1.07 g ceric ammonium nitrate in 10 ml water was added and stirred for another 20 minutes. After this time the mixture was poured into ice and extracted twice with dichloromethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426420B2
Source datasetuspto-grants-2013_04
ORD IDord-9576ce0d212f4a8b9a62fec9ac2b9827
Source noteuspto-grants-2013_04