Tributyltin Chloride → 1,2-Dimethyl-5-(tributylstannyl)-1H-imidazole

HRID 1888477Notes

Reaction equation

Br[C:2]1[N:6]([CH3:7])[C:5]([CH3:8])=[N:4][CH:3]=1.[CH2:9]([Sn:13]([CH2:19][CH2:20][CH2:21][CH3:22])([CH2:15][CH2:16][CH2:17][CH3:18])Cl)[CH2:10][CH2:11][CH3:12]>>[CH3:7][N:6]1[C:2]([Sn:13]([CH2:15][CH2:16][CH2:17][CH3:18])([CH2:19][CH2:20][CH2:21][CH3:22])[CH2:9][CH2:10][CH2:11][CH3:12])=[CH:3][N:4]=[C:5]1[CH3:8]

Participants

Reactant 2

HCID 15096Tributyltin Chloride

HCID 72048795-bromo-1,2-dimethyl-1H-imidazole

Product 1

HCID 128472111,2-Dimethyl-5-(tributylstannyl)-1H-imidazole

Procedure

The title compound was prepared following a similar procedure to previous example using 5-bromo-1,2-dimethyl-1H-imidazole and tributylchlorostannane.

Sources & evidence

ORD record: ord-6f17873999524c0da779a0afd2b800db
Source dataset: uspto-grants-2013_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08501765B2

Reaction notes

Loading…