5-(Chloromethyl)-1,2,3-trimethoxybenzene → 1-(3,4,5-Trimethoxybenzyl)-1-(2-thienyl)propyl isocyanide
Reaction equation
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH:6]([N+:9]#[C-:10])[CH2:7][CH3:8].[CH3:11][O:12][C:13]1[CH:14]=[C:15]([CH:18]=[C:19]([O:23][CH3:24])[C:20]=1[O:21][CH3:22])[CH2:16]Cl>>[CH3:11][O:12][C:13]1[CH:14]=[C:15]([CH:18]=[C:19]([O:23][CH3:24])[C:20]=1[O:21][CH3:22])[CH2:16][C:6]([N+:9]#[C-:10])([C:2]1[S:1][CH:5]=[CH:4][CH:3]=1)[CH2:7][CH3:8]Participants
3
Procedure
2.5 g of 1-(2-thienyl)propyl isocyanide and 4.4 g of 3,4,5-trimethoxybenzyl chloride are treated in the same manner as described in Example 1-(1) to give 3.7 g of 1-(3,4,5-trimethoxybenzyl)-1-(2-thienyl)propyl isocyanide as a colorless oil. yield; 67.5%
Sources & evidence
- ORD record
- ord-e42ac0c041404f05a6a9d1401b2b93d8
- Source dataset
- uspto-grants-1990_08
- Patent number
- US04946862
Reaction notes
Loading…