HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → 1-Pyrrolidinecarboxylicacid,3-hydroxy-2-methyl-,1,1-dimethylethylester,(2R,3S)-(9CI)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 59710338 | HCID 59710338 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Pyrrolidinecarboxylicacid,3-hydroxy-2-methyl-,1,1-dimethylethylester,(2R,3S)-(9CI) | HCID 45096721 | — |
Reaction Steps
Tetrabutyl ammonium fluoride (16.7 mL, 1N in THF, 16.73 mmol) was added to a solution of 1,1-dimethylethyl(2R,3S)-3-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}-2-methyl-1-pyrrolidinecarboxylate in THF and stirred for 16 hours at room temperature. The reaction mixture was concentrated under reduced pressure and purified by silica gel column chromatography to yield the title compound (1.55 g, 7.8 mmol). 1H NMR (400 MHz, DMSO-D6) δ ppm 1.0 (m, 3 H) 1.4 (s, 9 H) 1.6 (m, 1 H) 1.9 (m, 1 H) 3.3 (m, 2 H) 3.5 (m, 1 H) 3.8 (m, 1 H) 4.9 (s, 1 H). ES+=202.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07368453B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-454c5e344ce34c68bd0cb450cab9b13f |
| Source note | uspto-grants-2008_05 |