HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 67420607, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl azodicarboxylate | HCID 5363146 | — |
| Reactant | HCID 11312156 | HCID 11312156 | — |
| Reactant | HCID 178498943 | HCID 178498943 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67420607 | HCID 67420607 | 66.2% |
Reaction Steps
To a mixture of 6-benzyloxy-4-hydroxy-2-oxo-2H-thiochromene-3-carboxylic acid methyl ester (Compound 62 (h), 591 mg, 1.73 mmol) and 2-(tert-Butyl-diphenyl-silanyl)-ethanol (687 mg, 2.42 mmol) (prepared according to the procedure published in J. Org. Chem. 2005, 70(4), 1467-1470) in THF (7 mL) was added triphenylphosphine (634 mg, 2.42 mmol), and DIAD (489 mg, 2.42 mmol). The resultant mixture was stirred at rt for 3.5 h. After concentration, the crude residue was purified by silica gel chromatography (eluting with 0-75% EtOAc/hexanes) to provide the title compound (697 mg). 1H NMR (200 MHz, CDCl3): δ (ppm)=7.69-7.14 (m, 18H), 5.83 (s, 2H), 4.25-4.09 (m, 2H), 3.49 (s, 3H), 1.89-1.81 (m, 2H), 1.08 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09149476B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-b74d33e3c5184591acfb8b5d95487955 |
| Source note | uspto-grants-2015_10 |