Dimethyl Sulfoxide → HCID 131711716, compound

HRID 1448930Notes

Reaction equation

HRID 1448930 reaction equation
[O:1]([CH2:19][CH:20]([CH3:48])[CH2:21][CH2:22][CH2:23][C:24]([CH3:47])([OH:46])[C:25](=[O:45])[CH2:26][CH2:27][C:28]1([O:44][CH2:43][CH2:42][O:41]1)[CH2:29][O:30][S:31]([C:34]1[CH:40]=[CH:39][C:37]([CH3:38])=[CH:36][CH:35]=1)(=[O:33])=[O:32])[Si:2]([C:15]([CH3:18])([CH3:17])[CH3:16])([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C(OC(=O)C)(=O)C.[CH3:56][S:57]([CH3:59])=O>>[O:1]([CH2:19][CH:20]([CH3:48])[CH2:21][CH2:22][CH2:23][C:24]([CH3:47])([O:46][CH2:56][S:57][CH3:59])[C:25](=[O:45])[CH2:26][CH2:27][C:28]1([O:41][CH2:42][CH2:43][O:44]1)[CH2:29][O:30][S:31]([C:34]1[CH:40]=[CH:39][C:37]([CH3:38])=[CH:36][CH:35]=1)(=[O:33])=[O:32])[Si:2]([C:15]([CH3:18])([CH3:17])[CH3:16])([C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1)[C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1

Participants

4

Procedure

11-t-Butyldiphenylsiloxy-6,10-dimethyl-2,2-ethylenedioxy-6-hydroxy-5-oxo-1-tosyloxyundecane (1.15 g) is dissolved in dimethyl sulfoxide (8.15 ml), acetic anhydride (8.15 ml) is added and the resulting solution is stirred for 20 hours. The solvents are removed in vacuo below 70° C. and the residue is partitioned between ether and saturated sodium bicarbonate solution. The organic layer is washed with brine and dried (sodium sulfate). The solution is removed in vacuo to give 11-t-butyldiphenylsiloxy-6,10-dimethyl-2,2-ethylenedioxy-6-methylthiomethoxy-5-oxo-1-tosyloxyundecane (1.13 g, 91%) as a yellow oil; nmr (CDCl3,δ) 0.88 (d, CH3CH), 1.04 [s, CH3)3 --C], 1.28 (s, ##STR39## 2.17 (s, SCH3), 2.42 (s, CH3 --Ph), 3.42 (d, OCH2CH), 3.89 (s, OCH2CH2O and TsOCH2C), 4.41 (s, OCH2S), 7.2--7.9 (aromatic H).

Workup

  1. customThe solvents are removed in vacuo below 70° C.
  2. customthe residue is partitioned between ether and saturated sodium bicarbonate solution
  3. washThe organic layer is washed with brine
  4. dry with materialdried (sodium sulfate)
  5. customThe solution is removed in vacuo

Sources & evidence

ORD record
ord-95dfae48ce904c92861a64943403c06b
Source dataset
uspto-grants-1980_02
Patent number
US04188328

Reaction notes

Loading…