HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448930Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 131711716, compound
https://huagongshe.com/reaction/1448930
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 131711717 | HCID 131711717 | — |
| Product | HCID 131711716 | HCID 131711716 | 91% |
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 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).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04188328 |
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| Source dataset | uspto-grants-1980_02 |
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| ORD ID | ord-95dfae48ce904c92861a64943403c06b |
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| Source note | uspto-grants-1980_02 |
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