HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956177Generated: November 2, 2026
Dimethyl Disulfide → HCID 18662974, compound
https://huagongshe.com/reaction/1956177
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | Nitrilooxonium tetrafluoroborate | HCID 11137142 | — |
| Reactant | HCID 18662979 | HCID 18662979 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 18662974 | HCID 18662974 | — |
Reaction Steps
To a mixture of 1.0 g (3.5 mmol) of 5-(6-amino-2,2-dimethylindan-1-yl)-4-methylthiopyrimidine in 25 mL of dry acetonitrile at 5° C. was added with stirring 1.0 g (7.0 mmol) of nitrosonium tetrafluoroborate. After 30 min the resulting solution was poured with stirring into a solution of 20 g (0.20 mol) of dimethyl disulfide in 100 mL of acetonitrile. After 2 hr, 0.50 g of sodium methanethiolate was added and the reaction mixture was heated with stirring to 60° C. for 16 hr. The mixture was cooled and poured into 600 mL of ether with stirring. The ethereal phase was recovered and was washed with water (2×100 mL), dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure. The residue was purified by column chromatography on silica gel to obtain 500 mg (45 percent of theory) of the title compound as a light gold oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05780465 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-1516747364bb455aa901bcdffe44c4e5 |
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| Source note | uspto-grants-1998_07 |
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