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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045804Generated: October 26, 2026

Triphenylphosphine → Benzyl 4-[1-(4-chloro-3-methylphenyl)-1H-tetrazol-5-yl]piperidine-1-carboxylate

https://huagongshe.com/reaction/1045804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantAzidotrimethylsilaneHCID 78378—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantBenzyl 4-[(4-chloro-3-methyl-phenyl)carbamoyl]piperidine-1-carboxylateHCID 86685835—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 4-[1-(4-chloro-3-methylphenyl)-1H-tetrazol-5-yl]piperidine-1-carboxylateHCID 86685836—

Reaction Steps

The product from step A (840 mg, 2.171 mmol) and triphenylphosphine (1139 mg, 4.34 mmol) in THF (8.0 ml) was treated with diisopropylazodicarboxylate (0.844 ml, 4.34 mmol) and trimethylsilyl azide (0.574 ml, 4.34 mmol) at rt. The mixture was stirred at rt for 24 h, then quenched with aqueous saturated NaHCO3, and extracted with MTBE. The combined organic layers were concentrated. Purification of the resulting crude product on SiO2 (0 to 100% EtOAc, hexanes) afforded the title compound as a clear colorless oil. HPLC/MS: 412.2/414.1 (M+1); Rt=1.22 min (LC2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569299B2
Source datasetuspto-grants-2013_10
ORD IDord-2d8c3e79343c4082867961a545480751
Source noteuspto-grants-2013_10