19404-18-3 → 3-(Bromomethyl)-5-chloro-1-benzothiophene
Reaction equation
[Br:1][CH2:2][C:3]1[C:4]2[CH:16]=[C:15]([Cl:17])[CH:14]=[CH:13][C:5]=2[S:6][C:7]=1C(OCC)=O.ClC1C=CC2SC=C(C)C=2C=1>>[Br:1][CH2:2][C:3]1[C:4]2[CH:16]=[C:15]([Cl:17])[CH:14]=[CH:13][C:5]=2[S:6][CH:7]=1Participants
3
Procedure
Using the general procedure of Example 1, Method A, (iv), replacing ethyl-5-chloro-3-methylbenzo[b]thiophene-2-carboxylate with 5-chloro-3-methylbenzo[b]thiophene gave 2.78 g (57%) of 3-bromomethyl-5-chlorobenzo[b]thiophene: mp 126°-128° C.
Sources & evidence
- ORD record
- ord-83af5daa7af244ce9b16da5d27b431d8
- Source dataset
- uspto-grants-1991_01
- Patent number
- US04981848
Reaction notes
Loading…