HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703239Generated: October 28, 2026
Iodine → 3,3,12,12-Tetramethoxy-2,13-dioxa-7,8-dithia-3,12-disilatetradecane
https://huagongshe.com/reaction/703239
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | (3-Mercaptopropyl)trimethoxysilane | HCID 20473 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3,3,12,12-Tetramethoxy-2,13-dioxa-7,8-dithia-3,12-disilatetradecane | HCID 3757973 | — |
Reaction Steps
A 28% solution of sodium methylate in methanol (97.6 g. 0.51 mole) is diluted with methanol (100 ml), and thereto is added γ-mercaptopropyltrimethoxysilane (100 g, 0.51 mole). The temperature of the mixture raises in a certain degree owing to the mixing heat but return to room temperature after about 30 minutes. To the mixture is added in portions iodine (64.6 g. 0.51 mole) with stirring. In view of exothermic reaction, the reaction vessel is cooled with ice water. After completion of the addition of iodine, the brown mixture is allowed to stand at room temperature for 3 hours to give a clean liquid having pale yellow color. The reaction mixture is moved to a flask, and the methanol solvent is distilled off under reduced pressure with a rotary evaporator. The residue containing white crystals and pale yellow liquid is filtered to separate the oily liquid (86.4 g). This liquid is subjected to analyses of IR, H-NMR and UV spectra, and thereby, it is confirmed that the liquid product is bis[γ-(trimethoxysilyl)propyl ]disulfide of the formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04981937 |
|---|
| Source dataset | uspto-grants-1991_01 |
|---|
| ORD ID | ord-400445aa3d004851b2ca328b0ccacddc |
|---|
| Source note | uspto-grants-1991_01 |
|---|