HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-[4-(4-Fluoro-benzyloxy)-benzenesulfonylamino]-oxo-heptanoic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Hydroxy-2-pentanone | HCID 62484 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | [4-(4-Fluoro-benzyloxy)-benzenesulfonylamino]-acetic acid tert-butyl ester | HCID 54478351 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[4-(4-Fluoro-benzyloxy)-benzenesulfonylamino]-oxo-heptanoic acid tert-butyl ester | HCID 70213828 | 57.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329397B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-e60ef466ecab44a6be4714fc293b9687 |
| Source note | uspto-grants-2001_12 |