HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044280Generated: October 31, 2026
Trimethyltin chloride → HCID 58204743, compound
https://huagongshe.com/reaction/2044280
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyltin chloride | HCID 14016 | — |
| Reactant | HCID 58204929 | HCID 58204929 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58204743 | HCID 58204743 | 74% |
Reaction Steps
To a mixture of 1-(2-(tert-butyldimethylsilyloxy)-2-methylpropyl)-4-iodo-1H-imidazole in DCM was added ethylmagnesium bromide at −78° C. The temperature of the mixture was allowed to warm up to about 10° C. slowly and cooled again. Trimethyltin chloride was added dropwise at −78° C. After the addition, the temperature was allowed to slowly warm up to room temperature. The reaction mixture was pouted into saturate NH4Cl solution, then extracted with DCM. The organic phase was washed with water twice, dried over anhydrous Na2SO4, and concentrated to give 1-(2-(tert-butyldimethylsilyloxy)-2-methylpropyl)-4-(trimethylstannyl)-1H-imidazole (Yield=74%). LC-MS: m/z=419 [M+H+]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586574B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-9f942f4bc0714e8cb1a700d05b94e21e |
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| Source note | uspto-grants-2013_11 |
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