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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127558Generated: November 4, 2026

Dimethyl Sulfoxide → HCID 131711716, compound

https://huagongshe.com/reaction/127558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 131711717HCID 131711717—
ProductHCID 131711716HCID 13171171691%

Reaction Steps

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 solvent 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], ##STR29## 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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256644
Source datasetuspto-grants-1981_03
ORD IDord-ab6d5c48890c4c0d80a601b00d6ea5d8
Source noteuspto-grants-1981_03