HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850262Generated: October 30, 2026
Dimethoxymethane → HCID 19362524, compound
https://huagongshe.com/reaction/850262
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethoxymethane | HCID 8020 | — |
| Reactant | 1,2-Bis(methylsulfanyl)benzene | HCID 137575 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 19362524 | HCID 19362524 | 55.3% |
Reaction Steps
46 g (0.343 mol) of AlCl3 are suspended in 200 ml of 1,2-dichloroethane and, at 0° C., 9.1 g (0.12 mol) of formaldehyde dimethylacetal are added. Then 17.0 g (0.1 mol) of 1,2-bis-(methylthio)benzene are added dropwise and the suspension is heated to room temperature. When the starting material can no longer be detected by GC analysis, the solution is poured into ice/water and the organic phase is separated off and dried over magnesium sulfate. When the solvent has been distilled off, 12.1 g (55%) of 1,2-bis(methylthio)-4-chloromethyl-benzene are obtained in the form of a yellow oil. The 1H-NMR spectrum (CDCl3) of the compound is consistent with the suggested structure: 7.17-7.13, s and d, 3 aromatic H; 4.52, s, 2H; 2.44, s, CH3S and 2.43, s, CH3S.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06017675 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-7aa8a857cd1c43399926db7418297e15 |
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| Source note | uspto-grants-2000_01 |
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