Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | (3R,3aR,6R,6aS)-tert-Butyl 3-hydroxy-6-(tosyloxy)tetrahydro-2H-furo[3,2-b]pyrrole-4(5H)-carboxylate | HCID 59343397 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 67439721 | HCID 67439721 | 88% |
Reaction Steps
A stirred solution of tosylate (35b) (250 mg, 0.63 mmol) and sodium thiomethoxide [CAS 5188-07-8] (88 mg, 1.25 mmol) in 3 ml of DMA was heated under an atmosphere of argon in a sealed pressure vessel at 90° C. for 2 hours. The mixture was then allowed to cool to ambient temperature then an aqueous saturated solution of ammonium chloride (10 mL) was added. The aqueous phase was extracted with tert-butyl methyl ether (3×7 ml). The organic phase was dried (MgSO4), filtered and reduced in vacuo to leave an oil. Flash chromatography over silica, eluting with diethyl ether:pentane 2:1 gave thiomethylether (54) as colourless oil (0.152 g, 88%). TLC(Rf=0.29, Et2O:pentane 2:1), HPLC-MS 220.1 [M+2H−tBu]+, 573.2 [2M+H]+; δH (500 MHz, CDCl3) mixture of rotamers 1:1; 1.46 (4.5H, s, CCH3), 1.49 (4.5H, s, CCH3), 2.16 (3H, s, SCH3), 3.20 (1H, brs, BocNCH2), 3.47-4.05 (4H, m, OCH2CHOH, BocNCH2 and CHSCH3), 4.24-4.45 (2H, m, BocNCH and OCH2CHOH), 4.63 (1H, s, OCHCHSCH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07799791B2 |
|---|
| Source dataset | uspto-grants-2010_09 |
|---|
| ORD ID | ord-174f0212305c42abb303094f64861bde |
|---|
| Source note | uspto-grants-2010_09 |
|---|