1,1-Dibromoethane → 4,4-Dimethyl-2-(4'-tetrahydropyranyloxymethylbiphenyl-2-yl)oxazoline

HRID 975286

反応式

HRID 975286 の反応式
[Mg].BrC(Br)C.BrC1C=CC(C[C:12]2([O:18][C:19]3([CH2:25][C:26]4[CH:31]=[CH:30][C:29](Br)=[CH:28]C=4)CCCCO3)[CH2:17][CH2:16][CH2:15][CH2:14][O:13]2)=CC=1.[CH3:35][C:36]1([CH3:49])[CH2:40][O:39][C:38]([C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][C:42]=2OC)=[N:37]1.[Cl-].[NH4+]>O1CCCC1>[CH3:49][C:36]1([CH3:35])[CH2:40][O:39][C:38]([C:41]2[CH:46]=[CH:45][CH:44]=[CH:43][C:42]=2[C:30]2[CH:31]=[CH:26][C:25]([CH2:19][O:18][CH:12]3[CH2:17][CH2:16][CH2:15][CH2:14][O:13]3)=[CH:28][CH:29]=2)=[N:37]1

参加物

7

反応物 5

HCID 112011,1-DibromoethaneHCID 25517Ammonium ChlorideHCID 3331894,4-Dimethyl-2-(2-methoxyphenyl)oxazolineHCID 5462224Magnesium2 回HCID 699599014-Bromobenzyl-tetrahydropyranyl ether

生成物 1

HCID 153808764,4-Dimethyl-2-(4'-tetrahydropyranyloxymethylbiphenyl-2-yl)oxazoline収率 58%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

Tetrahybrofuran (15 ml) was added to 1.2 g (49.4 mmol) of flaky magnesium, followed by the addition of a small amount of dibromoethane under stirring. After the confirmation of bubbling, a solution of 11.0 g (40.6 mmol) of 4-bromobenzyl-tetrahydropyranyl ether in tetrahydrofuran (15 ml) was dropwise added thereto. After the confirmation of the dissolution of the magnesium, the resulting mixture was further stirred at room temperature for one hour. Then, a solution of 7.0 g (34.1 mmol) of 4,4-dimethyl-2-(2'-methoxyphenyl)oxazoline in tetrahydrofuran (5 ml) was dropwise added thereto, followed by stirring for 12 hours. The reaction liquid was poured into a saturated aqueous solution of ammonium chloride, followed by the extraction with chloroform. After washing with water and drying, vacuum concentration was conducted. The residue was purified by silica gel column chromatography (a n-hexane/ethyl acetate system) to give 6.61 g of the title compound as an oil (yield 58%).

後処理

  1. customAfter the confirmation of bubbling
  2. stirringthe resulting mixture was further stirred at room temperature for one hour
  3. stirringby stirring for 12 hours
  4. customThe reaction liquid
  5. extractionfollowed by the extraction with chloroform
  6. washAfter washing with water
  7. customdrying
  8. concentrationvacuum concentration
  9. customThe residue was purified by silica gel column chromatography (a n-hexane/ethyl acetate system)

出典と根拠

ORDレコード
ord-c084c56625ac42aba5e1c33ceb9b5849
出典データセット
uspto-grants-1997_03
特許番号
US05608068

関連ノート

読み込み中…