HuagongsheHuagongshe Chemistry Print Report · For research reference only
D-1,4-Dithiothreitol → Dimethyl-sulfamic acid 5-tert-butyl-4-mercapto-2-methyl-phenyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | D-1,4-Dithiothreitol | HCID 446094 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | Dimethyl-sulfamic acid 5-tert-butyl-2-methyl-4-thiocyanato-phenyl ester | HCID 10496539 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Dimethyl-sulfamic acid 5-tert-butyl-4-mercapto-2-methyl-phenyl ester | HCID 10662229 | — |
Reaction Steps
To a round bottom flask equipped with a magnetic stirrer and condenser were added 1.1 g (3.3 mmol) of dimethyl-sulfamic acid 5-tert-butyl-2-methyl-4-thiocyanato-phenyl ester (prepared in Example SSS), dithiothreitol (1.29 g, 8.35 mmol), EtOH (40 mL), and 0.02M KH2PO4 buffer solution (5 mL), respectively. The reaction was refluxed overnight. The mixture was then quenched with H2O (250 mL) and extracted with a 1:1 mixture of hexanes:Et2O. The organic layer was again washed with H2O and brine, dried (MgSO4) and concentrated. The residue was dried under high vacuum to yield the title compound. 1H NMR (CDCl3) δ 1.45 (s, 9 H), 2.25 (s, 3 H), 3.02 (s, 6 H), 3.57 (s, 1 H), 7.01 (s, 1 H), 7.28 (s, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05834506 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-0fc603a7f9a749d28b0d169bb4db6176 |
| Source note | uspto-grants-1998_11 |