HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474299Generated: October 26, 2026
Benzyltrimethylammonium hydroxide → 2-(2-Methanesulfinyl-2-methylsulfanyl-vinyl)-1,3-dimethyl-benzene
https://huagongshe.com/reaction/474299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyltrimethylammonium hydroxide | HCID 66854 | — |
| Reactant | Methyl (methylsulfinyl)methyl sulfide | HCID 99129 | — |
| Reactant | 2,6-Dimethylbenzaldehyde | HCID 583841 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(2-Methanesulfinyl-2-methylsulfanyl-vinyl)-1,3-dimethyl-benzene | HCID 86631265 | 68.3% |
Reaction Steps
To a solution of 2,6-dimethyl-benzaldehyde (14.6 g, 109 mmol) in 1,4-dioxane (24.7 mL) was added methyl methylsulfinylmethyl sulfide (13.5 g, 109 mmol) followed by benzyltrimethylammonium hydroxide (9.10 g, 54.4 mmol). The resulting mixture was heated at 80° C. After 16 h, the mixture was cooled to rt and concentrated. The resulting residue was purified by FCC to afford a yellow oil (17.9 g, 68%). MS (ESI): mass calcd. for C12H16OS2, 240.1; m/z found, 241.1 [M+H]+. 1H NMR (CDCl3): 7.71 (s, 1H), 7.19-7.13 (m, 1H), 7.07 (d, J=7.5 Hz, 2H), 2.82 (s, 3H), 2.24 (s, 6H), 2.06 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637527B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-17a6dec82e4f48ee8ed05f2ccf4415d9 |
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| Source note | uspto-grants-2014_01 |
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