C[O:2][C:3]1[CH:4]=[C:5]([CH:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][CH2:10]2)[CH:6]=[CH:7][CH:8]=1.ClCCl.B(Br)(Br)Br.C(=O)(O)[O-].[Na+]>ClCCl>[OH:2][C:3]1[CH:4]=[C:5]([CH:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][CH2:10]2)[CH:6]=[CH:7][CH:8]=1A 3.0 g portion of the (+)-3-(3-methoxyphenyl)indoline obtained in Reference Example 4 was dissolved in 30 ml of dichloromethane, and this solution was added dropwise to 40 ml of a boron tribromide dichloromethane solution (1 mole/liter) at -70° C. After stirring the solution at room temperature overnight, ice water was added, the pH was adjusted to 9 with sodium bicarbonate, and the mixture was extracted with a chloroform/ethanol mixed solvent. After drying and concentration, ether was added to the residue to precipitate crystals which were then collected by filtration to obtain 2.7 g of 3-(3-hydroxyphenyl)indoline.
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