HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isothiocyanatotrimethylsilane → (8-Thiocyanato-chroman-5-yloxy)-acetic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isothiocyanatotrimethylsilane | HCID 75297 | — |
| Reactant | (Chroman-5-yloxy)-acetic acid methyl ester | HCID 11322001 | — |
| Reactant | HCID 178525681 | HCID 178525681 | — |
| Solvent | 1,1,1,3,3,3-Hexafluoro-2-propanol | HCID 13529 | — |
| Product | (8-Thiocyanato-chroman-5-yloxy)-acetic acid methyl ester | HCID 11196728 | 50% |
Reaction Steps
A stirred solution of (chroman-5-yloxy)-acetic acid methyl ester (2.1 g, 9.4 mmol) and trimethylsilyl isothiocyanate (2 mL, 14.1 mmol) in 30 mL 1,1,1,3,3,3-hexafluoro-propan-2-ol under a N2 atmosphere was treated with phenyliodine(III) bis(trifluoroacetate). The reaction mixture stirred at room temperature for 1 h and concentrated in vacuo. Purification by flash column chromatography (gradient elution: 10% EtOAc/hexanes to 40% EtOAc/hexanes) gave the title compound (1.3 g, 50%) as a pale yellow solid. 400 MHz 1H NMR (DMSO-d6) δ 7.31 (d, 1H, J=8.8 Hz), 6.54 (d, 1H, J=8.8 Hz), 4.83 (s, 2H), 4.21 (t, 2H, J=4.9 Hz), 3.64 (s, 3H), 2.60 (t, 2H, J=6.4 Hz), 1.89 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06833380B2 |
| Source dataset | uspto-grants-2004_12 |
| ORD ID | ord-e73c6d3bb5894f8a84eec94f1205614c |
| Source note | uspto-grants-2004_12 |