反応式
[C:1]1([C@H:7]([C@@H:9]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[OH:10])[OH:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(N(CC)CC)C.C1(C)C=CC=CC=1.Cl[P:32](Cl)[C-:33]1[CH:37]=[CH:36][CH:35]=[CH:34]1.[C-:39]1([P:44](Cl)Cl)[CH:43]=[CH:42][CH:41]=[CH:40]1.[Fe+2:47]>C(OCC)C.C1COCC1>[C:11]1([C@@H:9]2[C@@H:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[O:8][P:32]([C-:33]3[CH:37]=[CH:36][CH:35]=[CH:34]3)[O:10]2)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[C-:39]1([P:44]2[O:8][C@H:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[C@@H:9]([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[O:10]2)[CH:43]=[CH:42][CH:41]=[CH:40]1.[Fe+2:47]参加物
実験手順
At −78° C., 651 mg (3.04 mmol) of (R,R)-hydrobenzoin is charged in a vessel together with 1.0 ml of abs. triethylamine (6.63 mmol) in 150 ml of abs. toluene. A solution of 425 mg (0.80 mmol) of 1,1′-bis(dichlorophosphino)ferrocene (X) in 25 ml of abs. THF is added dropwise within 2 h. Then, thawing is allowed slowly in a cooling bath over night with stirring. The solution obtained is completely freed from solvent, and the orange solid is taken up in 200 ml of abs. diethyl ether. Insolubles are separated off by filtration through a P4 frit with Celite 545® as a filtering aid. The clear orange filtrate is completely freed from solvent to obtain an orange solid. Analytical results: 1H NMR (d8-THF, 300 MHz): 7.40 (s) [8H], 7.36-7.30 (m) [6H], 7.29-7.23 (m) [4H], 7.22-7.11 (m) [6H], 5.05 (d) JH-P=8.1 Hz [2H], 4.95 (d) JH-P=9 Hz [2H], 4.82-4.60 (m) [8H]; 31P NMR (d8-THF, 121 MHz): 181.7 (s).
後処理
- waitThen, thawing is allowed slowly in a cooling bath over night
- customThe solution obtained
- customInsolubles are separated off by filtration through a P4 frit with Celite 545® as a filtering aid
- customto obtain an orange solid
- customAnalytical results
出典と根拠
- ORDレコード
- ord-7db29df5a770448d83a7d76c6a280285
- 出典データセット
- uspto-grants-2003_06
- 特許番号
- US06583305B1
関連ノート
読み込み中…