1,2-Dibromoethane → HCID 22314138, compound

HRID 270252Notes

Reaction equation

HRID 270252 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:12]3[CH:13]=[CH:14][C:15]([OH:17])=[CH:16][C:11]=3[S:10][N:9]=2)=[CH:4][CH:3]=1.[Br:18][CH2:19][CH2:20]Br>>[Br:18][CH2:19][CH2:20][O:17][C:15]1[CH:14]=[CH:13][C:12]2[C:8]([C:5]3[CH:4]=[CH:3][C:2]([Br:1])=[CH:7][CH:6]=3)=[N:9][S:10][C:11]=2[CH:16]=1

Participants

3

Reactant 2

HCID 78391,2-DibromoethaneHCID 1358479523-(4-Bromo-phenyl)-benzo[d]isothiazol-6-ol

Product 1

HCID 22314138HCID 22314138, compound

Procedure

In analogy to example 2.1, 3-(4-bromo-phenyl)-benzo[d]isothiazol-6-ol and 1,2-dibromoethane were converted to yield 6-(2-Bromo-ethoxy)-3-(4-bromo-phenyl)-benzo[d]isothiazole as off-white solid, 105° C., MS: 411 (M, 2Br).

Sources & evidence

ORD record
ord-57b6909b762044f7b6475573847a9204
Source dataset
uspto-grants-2008_11
Patent number
US07449483B2

Reaction notes

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