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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163315Generated: October 29, 2026

Tributylphosphine → HCID 23111742, compound

https://huagongshe.com/reaction/1163315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant3-Phenoxybenzyl alcoholHCID 26295—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantHCID 23111808HCID 23111808—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductHCID 23111742HCID 2311174260%

Reaction Steps

A solution of ethyl 8-hydroxy-2,3,4,5-tetrahydro-1-benzoxepine-4-carboxylate (0.189 g, 0.800 mmol), 3-phenoxybenzyl alcohol (0.240 g, 1.20 mmol) and tributylphosphine (0.299 mL, 1.20 mmol) in toluene (8 mL) was stirred under ice-cooling. 1,1′-(Azodicarbonyl)dipiperidine (0.279 g, 1.20 mmol) was added by small portions, and the mixture was stirred under nitrogen atmosphere at room temperature for 8 hr. Hexane (4 mL) was added to the reaction mixture, and the precipitated insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (5%-20% ethyl acetate/hexane) to give the title compound (0.20 g, yield 60%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820837B2
Source datasetuspto-grants-2010_10
ORD IDord-266844d0576d4071968d9950360b664f
Source noteuspto-grants-2010_10