Furan → HCID 20027406, compound
Reaction equation
C[Si]([O:5][C:6]1[C:11]([Cl:12])=[CH:10][C:9](I)=[CH:8][C:7]=1[Cl:14])(C)C.[O:15]1[CH:19]=[CH:18][CH:17]=[CH:16]1>>[Cl:14][C:7]1[CH:8]=[C:9]([C:16]2[O:15][CH:19]=[CH:18][CH:17]=2)[CH:10]=[C:11]([Cl:12])[C:6]=1[OH:5]Participants
3
Procedure
2,6-Dichloro-4-(2-furanyl)phenol [IV; R1 =2-Cl, R2 =6-Cl, Het=2-furanyl] was prepared from 2,6-dichloro-4-iodophenyl trimethylsilyl ether and furan according to the procedure of Example 1(b), and was obtained in 52% yield as a light brown solid, m.p. 68-70° C.
Workup
- customwas obtained in 52% yield as a light brown solid, m.p. 68-70° C.
Sources & evidence
- ORD record
- ord-d4cd48d779ae4e329d1484a5193b2f7b
- Source dataset
- uspto-grants-1989_08
- Patent number
- US04857539
Reaction notes
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