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Hydrochloric Acid → HCID 67777371、化合物

HRID 1430744
ノート
印刷プレビュー

反応式

HRID 1430744 の反応式
[CH:1]12[O:10][CH:7]([CH:8]=[CH:9]1)[CH:6]1[CH:2]2[C:3](=[O:12])[CH2:4][C:5]1=[O:11].N1C2C(=CC=C3C=2N=CC=C3)C=CC=1.C([O-])(=O)C.C([O-])(=O)C.C([O-])(=O)C.[Cl:39][C:40]1[CH:53]=[CH:52][C:43]([C:44]2[CH:45]=[CH:46][C:47]([CH3:51])=[C:48]([Pb+3])[CH:49]=2)=[CH:42][CH:41]=1.Cl>C(OCC)(=O)C.C1(C)C=CC=CC=1>[Cl:39][C:40]1[CH:41]=[CH:42][C:43]([C:44]2[CH:45]=[CH:46][C:47]([CH3:51])=[C:48]([CH:4]3[C:3](=[O:12])[CH:2]4[CH:6]([CH:7]5[O:10][CH:1]4[CH:9]=[CH:8]5)[C:5]3=[O:11])[CH:49]=2)=[CH:52][CH:53]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 13181,10-PhenanthrolineHCID 2067932010-Oxa-tricyclo[5.2.1.0*2,6*]dec-8-ene-3,5-dioneHCID 178476525HCID 178476525、化合物

生成物 1

HCID 67777371HCID 67777371、化合物

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒
HCID 8857
Ethyl Acetate
溶媒

実験手順

To a mixture of (1RS,2SR,6RS,7SR)-10-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione (374 mg, 2.3 mmol) and phenanthroline (610 mg, 5 mmol) under an atmosphere of nitrogen is added dry toluene (20 ml) and 4′-chloro-4-methylbiphen-3-yllead triacetate (2.0 g, 3.4 mmol). The reaction mixture is heated at reflux for 3.5 hours, then cooled to room temperature, acidified to pH1 with 2N aqueous hydrochloric acid (20 ml), ethyl acetate (20 ml) added and the mixture is filtered to remove solids. The filtrate is poured into a separating funnel and extracted with ethyl acetate. The organic extracts are combined, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The crude product is purified by column chromatography on silica gel to give (1RS,2SR,6RS,7SR)-4-(4′-chloro-4-methylbiphenyl-3-yl)-10-oxatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione.

後処理

  1. temperatureThe reaction mixture is heated
  2. temperatureat reflux for 3.5 hours
  3. additionadded
  4. filtrationthe mixture is filtered
  5. customto remove solids
  6. additionThe filtrate is poured into a separating funnel
  7. extractionextracted with ethyl acetate
  8. dry with materialdried over anhydrous magnesium sulfate
  9. filtrationfiltered
  10. customthe filtrate is evaporated under reduced pressure
  11. customThe crude product is purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-4cf0a6eea0cf423781420c1640f7e618
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08940913B2

反応ノート

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