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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530449Generated: November 2, 2026

Trimethyltin chloride → HCID 58204743, compound

https://huagongshe.com/reaction/1530449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyltin chlorideHCID 14016—
ReactantHCID 58204929HCID 58204929—
ReactantHCID 178418443HCID 178418443—
SolventDichloromethaneHCID 6344—
ProductHCID 58204743HCID 5820474374%

Reaction Conditions

Temperature10 °C

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+] 1H NMR (CDCl3, 400 MHz): δ 7.63 (s, 1H), 7.00 (s, 1H), 3.79 (s, 2H), 1.22-1.19 (s, 6H), 0.86 (s, 9H), 0.27 (s, 6H), 0.02 (s, 6H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09090628B2
Source datasetuspto-grants-2015_07
ORD IDord-a2457e7eef2a4999896b0569f65a0acd
Source noteuspto-grants-2015_07