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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269321Generated: October 29, 2026

Triphenylphosphine → 2-[4-(4-Fluoro-benzyloxy)-benzenesulfonylamino]-oxo-heptanoic acid tert-butyl ester

https://huagongshe.com/reaction/2269321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-Hydroxy-2-pentanoneHCID 62484—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant[4-(4-Fluoro-benzyloxy)-benzenesulfonylamino]-acetic acid tert-butyl esterHCID 54478351—
SolventTetrahydrofuranHCID 8028—
Product2-[4-(4-Fluoro-benzyloxy)-benzenesulfonylamino]-oxo-heptanoic acid tert-butyl esterHCID 7021382857.7%

Reaction Steps

To a mixture of acetyl propanol (0.39 mL, 3.8 mmol), [4-(4-fluoro-benzyloxy)-benzenesulfonylamino]-acetic acid tert-butyl ester (1.0 g, 2.53 mmol) and tetrahydrofuran (8 mL) was added triphenylphosphine (1.0 g, 3.8 mmol) and diethylazodicarboxylate (0.60 mL, 3.8 mmol). After stirring for 6 h at room temperature, the mixture was treated with additional acetyl propanol (0.15 mL), triphenyl phosphine (0.30 g) and diethylazodicarboxylate (0.20 mL). After stirring for 30 min, the mixture was concentrated in vacuo, and the residue was purified by silica gel chromatography eluting with 4:1 to 2:1 hexane-ethyl acetate, giving 0.70 g of 2-[4-(4-fluoro-benzyloxy)-benzenesulfonylamino]-oxo-heptanoic acid tert-butyl ester as a colorless solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329397B1
Source datasetuspto-grants-2001_12
ORD IDord-e60ef466ecab44a6be4714fc293b9687
Source noteuspto-grants-2001_12