2-Fluoroethyl bromide → HCID 86601080, compound
Reaction equation
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:19])=[C:6]([CH2:8][C:9]2[S:13][C:12]3[CH:14]=[CH:15][C:16]([OH:18])=[CH:17][C:11]=3[CH:10]=2)[CH:7]=1.Br[CH2:21][CH2:22][F:23]>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:19])=[C:6]([CH2:8][C:9]2[S:13][C:12]3[CH:14]=[CH:15][C:16]([O:18][CH2:21][CH2:22][F:23])=[CH:17][C:11]=3[CH:10]=2)[CH:7]=1Participants
3
Procedure
5-Bromo-1-(5-methoxybenzo[b]thiophene-2-yl methyl)-2-methylbenzene obtained in Reference Example 158 was treated in a manner similar to Reference Example 132-(1) to give 5-bromo-1-(5-hydroxybenzo[b]thiophen-2-ylmethyl)-2-methylbenzene as colorless powder. ESI-Mass m/Z 331/333 (M−H). (2) The above 5-bromo-1-(5-hydroxybenzo[b]thiophen-2-ylmethyl)-2-methylbenzene and 1-bromo-2-fluoroethane were treated in a manner similar to Reference Example 132-(2) to give the desired 5-bromo-1-(5-(2-fluoroethyloxy)benzo[b]thiophene-2-ylmethyl)-2-methylbenzene.
Sources & evidence
- ORD record
- ord-181417c9957348309a045d112ec48714
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08222219B2
Reaction notes
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