HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4,4,6,6-Tetramethyl-4,6-dihydrofuro[3,4-d]thiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 4-Bromo-2,2,5,5-tetramethyldihydrofuran-3(2h)-one | HCID 12201745 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4,4,6,6-Tetramethyl-4,6-dihydrofuro[3,4-d]thiazol-2-amine | HCID 79006302 | — |
Reaction Steps
To a solution of Example 248A (10.0 g, 0.045 mol) in ethanol (100 mL) were added thiourea (3.8 g, 0.05 mol) and triethylamine (6.3 mL, 0.045 mol). The reaction mixture was heated at reflux overnight, then cooled, and concentrated under reduced pressure. The residue was diluted with water (25 mL) and extracted with ethyl acetate (3×50 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated. The residue was purified by column chromatography (SiO2, 0-5% methanol in CH2Cl2) to afford the title compound. MS (ESI+) m/z 199 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841334B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-8fcb8b0e9d8d40428d516bffd4312d71 |
| Source note | uspto-grants-2014_09 |