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Iodine chloride → 7-fluoro-6-iodo-3,4-dihydro-2H-1,4-benzoxazin-3-one

HRID 277667
ノート
印刷プレビュー

反応式

HRID 277667 の反応式
[F:1][C:2]1[CH:12]=[CH:11][C:5]2[NH:6][C:7](=[O:10])[CH2:8][O:9][C:4]=2[CH:3]=1.[I:13]Cl.S(=O)(O)[O-].[Na+]>C(O)(=O)C>[I:13][C:12]1[C:2]([F:1])=[CH:3][C:4]2[O:9][CH2:8][C:7](=[O:10])[NH:6][C:5]=2[CH:11]=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 24640Iodine chlorideHCID 137312957-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 23665763Sodium Bisulfite

生成物 1

HCID 226256087-fluoro-6-iodo-3,4-dihydro-2H-1,4-benzoxazin-3-one収率 94.9%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

7-Fluoro-2H-1,4-benzoxazin-3(4H)-one (15.8 g) was mixed with iodine monochloride (15.6 g) in acetic acid (150 ml) and heated to reflux for 36 h. The cooled mixture was treated with saturated aqueous sodium bisulfite until the color was dissipated. The solid was filtered and washed well with water. The solid was air dried and dried further by dissolution in dimethylformamide (100 ml) and evaporated to dryness under reduced pressure to give the desired product (26.3 g) contaminated with some starting material. (The reaction can be taken to completion by addition of more iodine monochloride and refluxing for 24 h longer.) The crude product was used in Step B.

後処理

  1. temperatureheated
  2. temperatureto reflux for 36 h
  3. filtrationThe solid was filtered
  4. washwashed well with water
  5. customdried
  6. dry with materialdried further by dissolution in dimethylformamide (100 ml)
  7. customevaporated to dryness under reduced pressure

出典と根拠

ORDレコード
ord-e41b3f56f6d64b44836610ae62f0fc1c
出典データセット
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06358885B1

反応ノート

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