Chlorine → HCID 69517866, compound
Reaction equation
[OH:1][CH2:2][C:3]([C:6]1[CH:15]=[C:14]2[C:9]([CH:10]=[C:11]([C:20]([O:22][CH2:23][CH3:24])=[O:21])[CH:12]([C:16]([F:19])([F:18])[F:17])[O:13]2)=[CH:8][CH:7]=1)([CH3:5])[CH3:4].[Cl:25]Cl>CCOC(C)=O.C(Cl)Cl>[Cl:25][C:7]1[CH:8]=[C:9]2[C:14](=[CH:15][C:6]=1[C:3]([CH3:5])([CH3:4])[CH2:2][OH:1])[O:13][CH:12]([C:16]([F:18])([F:19])[F:17])[C:11]([C:20]([O:22][CH2:23][CH3:24])=[O:21])=[CH:10]2Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A single treatment of ethyl 7-(2-hydroxy-1,1-dimethylethyl)-2-(trifluoromethyl)-2H-chromene-3-carboxylate (5.4 g 16 mmoles) with Cl2 was performed as described in Example 115 Step 2. Chromatography of the residue using a gradient of 0-10% EtOAc—DCM as eluent gave the title compound, 3.7 g, as a nearly colorless oil.
Sources & evidence
- ORD record
- ord-98a2aeff858943598fea3e25aa258be1
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07259266B2
Reaction notes
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