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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277182Generated: October 31, 2026

Triphenylphosphine → HCID 86731239, compound

https://huagongshe.com/reaction/2277182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamateHCID 7023103—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
ReactantDIAD tolueneHCID 66880968—
ReactantHCID 86731237HCID 86731237—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86731239HCID 8673123953.9%

Reaction Steps

To a solution of 2-(4-(cyclopropylmethoxy)-3-fluorophenyl)-7-fluoro-1,3-benzoxazol-6-ol (3.96 g), tert-butyl ((2S)-1-hydroxypropan-2-yl)carbamate (3.28 g) and triphenylphosphine (4.91 g) in THF (50 mL) was added dropwise diisopropyl azodicarboxylate toluene solution (1.9 M, 9.85 mL) at 0° C., and the mixture was stirred at room temperature for 30 min. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (NH, hexane/ethyl acetate) to give a solid. To this solid was added 4 M hydrogen chloride/ethyl acetate (50 mL), and the mixture was stirred at room temperature for 10 min, and concentrated. To the residue were added pyridine (50 mL) and acetic anhydride (50 mL), and the mixture was stirred at room temperature for 15 min. The reaction mixture was concentrated under reduced pressure, and the obtained solid was dissolved in ethyl acetate/methanol, and the solution was subjected to silica gel column chromatography (NH, ethyl acetate), and concentrated. The obtained solid was recrystallized (hexane/ethyl acetate) to give the title compound as white crystals (2.80 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133129B2
Source datasetuspto-grants-2015_09
ORD IDord-4a6e170bef584ad8b7b294d64156625a
Source noteuspto-grants-2015_09