HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium amide → 2,2,6,6-Tetramethyl-4-piperidinyl t-butyl-sulphonyl-acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium amide | HCID 24532 | — |
| Reactant | 4-Hydroxy-2,2,6,6-tetramethylpiperidine | HCID 75471 | — |
| Reactant | Methyl 2-(2-methylpropane-2-sulfonyl)acetate | HCID 43444477 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2,2,6,6-Tetramethyl-4-piperidinyl t-butyl-sulphonyl-acetate | HCID 54332638 | — |
Reaction Steps
38.8 g (0.2 mol) of methyl t-butylsulphonyl-acetate, prepared according to the method of von Leusen and Strating, Rec. Trav, Chim. 84, 140 (1965), and 31.4 g (0.2 mol) of 4-hydroxy-2,2,6,6-tetramethylpiperidine are dissolved in 50 ml of xylene. The mixture is warmed to 130°, 0.2 g of lithium amide in 50 ml of xylene is added and the mixture is stirred for 12 hours at 130°-140°. The xylene is removed in vacuo and the residue is distilled to give 2,2,6,6-tetramethyl-4-piperidinyl t-butyl-sulphonyl-acetate; yield: 33.7 grams, boiling point 153°-154°/10-3 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04148784 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-e699c697c18f4bd396844235484c158f |
| Source note | uspto-grants-1979_04 |