反応式
[CH2:1]([O:8][C:9]1[CH:18]=[C:17]([I:19])[CH:16]=[CH:15][C:10]=1[C:11](OC)=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CC(C[AlH]CC(C)C)C>C1(C)C=CC=CC=1>[CH2:1]([O:8][C:9]1[CH:18]=[C:17]([I:19])[CH:16]=[CH:15][C:10]=1[CH2:11][OH:12])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
4
実験手順
The procedure is the same as that described above, using 14 g of methyl 2-benzyloxy-4-iodobenzoate, 350 ml of toluene and 72 ml of DiBAlH. The product is purified by chromatography on a silica column, eluted with a heptane/ethyl acetate 9:1 mixture. After evaporation of the solvents, 12.2 g (99%) of the expected compound are recovered in the form of a yellow oil.
後処理
- customThe product is purified by chromatography on a silica column
- washeluted with a heptane/ethyl acetate 9:1 mixture
- customAfter evaporation of the solvents, 12.2 g (99%) of the expected compound
- customare recovered in the form of a yellow oil
出典と根拠
- ORDレコード
- ord-6be7912f618e4550a1e5a34776ba1fef
- 出典データセット
- uspto-grants-2010_11
- 特許番号
- US07829588B2
関連ノート
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