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Hydrochloric Acid → Dibenzylmethylene(cyclopentadienyl)(2,7-di[2-naphthyl]-3,6-ditert-butylfluorene)

HRID 1050658
ノート
印刷プレビュー

反応式

HRID 1050658 の反応式
[C:1](OC)([CH3:4])([CH3:3])[CH3:2].[CH:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[CH:9][C:8]=1[C:17]1[C:29]([C:30]([CH3:33])([CH3:32])[CH3:31])=[CH:28][C:27]2[C:26]3[C:21](=[CH:22][C:23]([C:38]4[CH:47]=[CH:46][C:45]5[C:40](=[CH:41][CH:42]=[CH:43][CH:44]=5)[CH:39]=4)=[C:24]([C:34]([CH3:37])([CH3:36])[CH3:35])[CH:25]=3)[CH2:20][C:19]=2[CH:18]=1.[CH2:48]([Li])[CH2:49][CH2:50][CH3:51].Cl>C(OCC)C.CCCCCC>[CH2:2]([C:51](=[C:28]1[C:27]2[C:19]([CH:20]=[C:21]3[C:26]=2[CH:25]=[C:24]([C:34]([CH3:37])([CH3:36])[CH3:35])[C:23]([C:38]2[CH:47]=[CH:46][C:45]4[C:40](=[CH:41][CH:42]=[CH:43][CH:44]=4)[CH:39]=2)=[CH:22]3)=[C:18]([CH:21]2[CH:26]=[CH:27][CH:19]=[CH:20]2)[C:17]([C:8]2[CH:9]=[CH:10][C:11]3[C:16](=[CH:15][CH:14]=[CH:13][CH:12]=3)[CH:7]=2)=[C:29]1[C:30]([CH3:31])([CH3:32])[CH3:33])[CH2:50][C:49]1[CH:48]=[CH:16][CH:7]=[CH:8][CH:9]=1)[C:1]1[CH:4]=[CH:10][CH:11]=[CH:12][CH:3]=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 15413tert-Butyl methyl etherHCID 866231922,7-Di(2-naphthyl)-3,6-ditert-butyl-fluoreneHCID 178418339Butyllithium

生成物 1

HCID 131736077Dibenzylmethylene(cyclopentadienyl)(2,7-di[2-naphthyl]-3,6-ditert-butylfluorene)収率 53%

試薬・触媒・溶媒 2

HCID 3283
Diethyl Ether
溶媒
HCID 8058Hexane溶媒

実験手順

Under a nitrogen atmosphere, 80 mL of dehydrated tert-butylmethylether was added to 0.82 g (1.54 mmol) of 2,7-di(2-naphthyl)-3,6-ditert-butyl-fluorene, and the mixture was stirred. This solution was cooled in an ice bath, and 1.10 mL (1.76 mmol) of a 1.60 mol/L hexane solution of n-butyllithium was added. The mixture was stirred at room temperature for 22 hours. To the yellow suspension thus obtained, 0.44 g (1.70 mmol) of 6,6-dibenzofulvene synthesized in Synthesis Example 1-1 (iii) was added, and the mixture was heated to reflux for 19 hours. Subsequently, 30 mL of 1N hydrochloric acid was added to the light orange-brown solution obtained to terminate the reaction. Then, 100 mL of diethylether was added to perform a liquid-liquid phase separation, and the soluble fraction was extracted. This organic layer was washed two times with a saturated aqueous solution of sodium hydrogen carbonate, two times with water, and once with saturated brine, and then dried over magnesium sulfate. The solvent was distilled off, and the residue was purified by column chromatography to obtain a target product as a pale yellow solid (yield 0.64 g (53%)). The target product was identified by 1H-NMR and FD-MS spectroscopy.

後処理

  1. temperatureThis solution was cooled in an ice bath
  2. stirringThe mixture was stirred at room temperature for 22 hours
  3. customTo the yellow suspension thus obtained
  4. additionwas added
  5. temperaturethe mixture was heated
  6. temperatureto reflux for 19 hours
  7. customobtained
  8. customto terminate
  9. customthe reaction
  10. customa liquid-liquid phase separation
  11. extractionthe soluble fraction was extracted
  12. washThis organic layer was washed two times with a saturated aqueous solution of sodium hydrogen carbonate, two times with water
  13. dry with materialonce with saturated brine, and then dried over magnesium sulfate
  14. distillationThe solvent was distilled off
  15. customthe residue was purified by column chromatography

出典と根拠

ORDレコード
ord-7364c66e938e434c8b8f8f9ebf3ec2c7
出典データセット
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09382356B2

反応ノート

読み込み中…

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