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Hydrochloric Acid → HCID 69029202、化合物

HRID 1868572
ノート
印刷プレビュー

反応式

HRID 1868572 の反応式
C[Si](C)(C)N[Si](C)(C)C.[Li].[CH3:11][C:12]([C:14]1[CH:15]=[CH:16][C:17]([OH:21])=[CH:18][C:19]=1[OH:20])=[O:13].C([O:24][C:25](=O)[C:26]1[CH:31]=[C:30]([O:32][CH2:33][C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)[CH:29]=[C:28]([O:40][CH2:41][C:42]2[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=2)[CH:27]=1)C.Cl>O1CCCC1>[CH2:41]([O:40][C:28]1[CH:27]=[C:26]([C:25](=[O:24])[CH2:11][C:12]([C:14]2[CH:15]=[CH:16][C:17]([OH:21])=[CH:18][C:19]=2[OH:20])=[O:13])[CH:31]=[C:30]([O:32][CH2:33][C:34]2[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=2)[CH:29]=1)[C:42]1[CH:43]=[CH:44][CH:45]=[CH:46][CH:47]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 69902',4'-DihydroxyacetophenoneHCID 3016563Ethyl 3,5-bis(benzyloxy)benzoateHCID 57426343Lithium bis(trimethylsilyl)amide

生成物 1

HCID 69029202HCID 69029202、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒3 回

反応条件

温度
-30 °C

実験手順

A solution of 20% lithiumhexamethyldisilazane in tetrahydrofuran (217.5 mL, 260 mmol) was added to a well-stirred solution of 2,4-dihydroxy acetophenone, 14 (9.88 g, 65 mmol) in tetrahydrofuran (150 mL) under nitrogen atmosphere at −78° C. for 30 min. The reaction mixture was stirred at −78° C. for 1 h and at −30° C. for 2 h. It was again cooled to −78° C. and a solution of ethyl-3,5-dibenzyloxy-benzoate 8 (23.5 g, 65 mmol) in tetrahydrofuran (100 mL) was added over a period of 30 min. It was further stirred at room temperature for overnight and poured into ice water containing hydrochloric acid. It was extracted with chloroform, dried over sodium sulphate, filtered and evaporated on rotavapor to afford 1-(3,5-bis-benzyloxy-phenyl)-3-(2,4-dihydroxy-phenyl)-propane-1,3-dione (16). The residue, 16 (37.8 g) was refluxed with Dowex-H+ (8 g) in 2-propanol (300 mL) for 34 h. 2-Propanol was evaporated on rotavapor, residue suspended in hot dimethyl formamide and filtered. The filtrate was 3,4-Dimethoxy-benzoic acid (10). Yield 2 g (8%); mp 179-181° C.; MS (FAB) 183 (M++1); IR (KBr) 2939, 2836, 1867, 1678; 1H NMR (200 MHz, CDCl3) δ 7.79 (dd, J=8.4 Hz, 1.9 Hz, 1H), 7.60 (d, J=1.8 Hz, 1H), 6.93 (d, J=8.5 Hz, 1H), 3.96 (s, 6H).

後処理

  1. temperatureIt was again cooled to −78° C.
  2. stirringIt was further stirred at room temperature for overnight
  3. extractionIt was extracted with chloroform
  4. dry with materialdried over sodium sulphate
  5. filtrationfiltered
  6. customevaporated on rotavapor

出典と根拠

ORDレコード
ord-1fe4fdc7c90c406d9fcff0e89dbbb623
出典データセット
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07635779B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート