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Benzoic Acid → HCID 178441401、化合物

HRID 1493675
ノート
印刷プレビュー

反応式

HRID 1493675 の反応式
C(=O)([O-])[O-].[Ba+2].[C:6]([OH:14])(=[O:13])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH3:15][CH2:16][CH2:17][CH2:18][CH:19]1[C:54](=[O:55])[O:53][CH:52]([CH:56]([CH:58]([OH:66])[CH2:59][CH2:60][CH2:61][NH:62][C:63]([NH2:65])=[NH:64])[CH3:57])[CH:51]([CH3:67])[CH:50]=[C:49]([CH3:68])[CH2:48][CH2:47][CH2:46][CH2:45][CH:44]([OH:69])[CH2:43][CH:42]([OH:70])[CH2:41][CH:40]([OH:71])[CH2:39][CH:38]([OH:72])[CH2:37][CH:36]([OH:73])[CH:35]([O:74][C@H:75]2[O:79][C@H:78]([CH2:80][OH:81])[C@@H:77]([OH:82])[C@@H:76]2[OH:83])[CH:34]=[C:33]([CH3:84])[CH:32]([OH:85])[CH2:31][CH2:30][CH2:29][CH:28]([OH:86])[CH2:27][CH2:26][CH2:25][CH:24]([OH:87])[CH2:23][CH2:22][CH:21]([CH3:88])[CH:20]1[OH:89].S([O-])([O-])(=O)=O>CO>[CH3:15][CH2:16][CH2:17][CH2:18][CH:19]1[C:54](=[O:55])[O:53][CH:52]([CH:56]([CH:58]([OH:66])[CH2:59][CH2:60][CH2:61][NH:62][C:63]([NH2:65])=[NH:64])[CH3:57])[CH:51]([CH3:67])[CH:50]=[C:49]([CH3:68])[CH2:48][CH2:47][CH2:46][CH2:45][CH:44]([OH:69])[CH2:43][CH:42]([OH:70])[CH2:41][CH:40]([OH:71])[CH2:39][CH:38]([OH:72])[CH2:37][CH:36]([OH:73])[CH:35]([O:74][C@H:75]2[O:79][C@H:78]([CH2:80][OH:81])[C@@H:77]([OH:82])[C@@H:76]2[OH:83])[CH:34]=[C:33]([CH3:84])[CH:32]([OH:85])[CH2:31][CH2:30][CH2:29][CH:28]([OH:86])[CH2:27][CH2:26][CH2:25][CH:24]([OH:87])[CH2:23][CH2:22][CH:21]([CH3:88])[CH:20]1[OH:89].[C:6]([O-:14])(=[O:13])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 243Benzoic AcidHCID 10563Barium CarbonateHCID 178441404HCID 178441404、化合物

生成物 1

HCID 178441401HCID 178441401、化合物収率 92.1%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

0.087 g (0.444 millimole) of barium carbonate are suspended in 15 ml of methanol whereupon 0.11 g (0.91 millimole) of benzoic acid is added. The suspension thus obtained is heated to boiling until a clear solution is obtained. The clear and colorless solution is added to a suspension of 1.0 g (0.887 millimoles) of primycin sulfate and 80 ml of methanol and the reaction mixture is heated to boiling for 20 minutes under stirring. The hot solution is filtered through Celite and the filtrate is evaporated to dryness in vacuo. The residue is treated with ether, filtered and the solid is washed on the filter with 15 ml of a 2:1 mixture of acetone and water. Thus 0.98 g of primycin benzoate is obtained in the form of a white powder, yield 90.6%. Mp.: 170°-171° C., /α/D25 =+36.9°.

後処理

  1. additionis added
  2. customThe suspension thus obtained
  3. temperatureis heated
  4. customis obtained
  5. temperaturethe reaction mixture is heated
  6. filtrationThe hot solution is filtered through Celite
  7. customthe filtrate is evaporated to dryness in vacuo
  8. additionThe residue is treated with ether
  9. filtrationfiltered
  10. washthe solid is washed on the
  11. filtrationfilter with 15 ml of a 2:1 mixture of acetone and water

出典と根拠

ORDレコード
ord-7acba07a52094cf58b09aac16147d96e
出典データセット
uspto-grants-1991_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05023242

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート