Acetonitrile → HCID 86660546、化合物

HRID 333112

反応式

HRID 333112 の反応式
[C:1]([O:6]C(=O)C(C)=C)(=[O:5])[C:2]([CH3:4])=[CH2:3].C(#N)C.[Br:15][C:16]([F:26])([F:25])[C:17]([F:24])([F:23])[CH2:18][CH2:19][CH2:20][CH2:21]O.C(N(CC)CC)C>O>[C:1]([OH:6])(=[O:5])[C:2]([CH3:4])=[CH2:3].[Br:15][C:16]([F:25])([F:26])[C:17]([F:23])([F:24])[CH2:18][CH2:19][CH2:20][CH3:21]

参加物

6

実験手順

A 300 mL reactor was charged under nitrogen with 18.2 g (119 mmol/1.5 equivalents) of methacrylic anhydride and 150 mL of acetonitrile, followed by putting it in an ice bath. 20.0 g (79.0 mmol/1.0 equivalent) of 6-bromo-5,5,6,6-tetrafluorohexan-1-ol was added thereto, followed by adding dropwise of 12.0 g (119 mmol/1.5 equivalents) of triethylamine. After the dropping, stirring was conducted at 60 degrees for 10 hours. Then, 100 mL of water was added, and extraction was conducted two times with 200 mL of diisopropyl ether. The obtained organic layer was washed further with diluted hydrochloric acid, sodium bicarbonate water and brine, followed by removing water by sodium sulfate and conducting filtration. Then, isopropyl ether was distilled out, thereby obtaining 23.8 g of the target 6-bromo-5,5,6,6-tetrafluorohexane methacrylate. Upon this, purity was 96%, and yield was 90%.

後処理

  1. extractionextraction
  2. washThe obtained organic layer was washed further with diluted hydrochloric acid, sodium bicarbonate water and brine
  3. customby removing water by sodium sulfate
  4. filtrationfiltration
  5. distillationThen, isopropyl ether was distilled out

出典と根拠

ORDレコード
ord-1b990a540b2c470e917e76b793280537
出典データセット
uspto-grants-2014_11
特許番号
US08877960B2

関連ノート

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