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Water → Ethyl difluoro(6-methylpyridazin-3-yl)acetate

HRID 1357943
ノート
印刷プレビュー

反応式

HRID 1357943 の反応式
[F:1][C:2]([F:9])(I)[C:3]([O:5][CH2:6][CH3:7])=[O:4].Br[C:11]1[N:12]=[N:13][C:14]([CH3:17])=[CH:15][CH:16]=1.O.[NH4+].[Cl-]>CS(C)=O.[Cu]>[F:1][C:2]([F:9])([C:11]1[N:12]=[N:13][C:14]([CH3:17])=[CH:15][CH:16]=1)[C:3]([O:5][CH2:6][CH3:7])=[O:4]
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 962WaterHCID 25517Ammonium ChlorideHCID 2737200Ethyl difluoro(iodo)acetateHCID 119590863-Bromo-6-methylpyridazine

生成物 1

HCID 69558022Ethyl difluoro(6-methylpyridazin-3-yl)acetate収率 97.1%

試薬・触媒・溶媒 2

HCID 23978Copper触媒
HCID 679
Dimethyl Sulfoxide
溶媒
2 回

実験手順

This procedure is derived from the general method of T. Taguchi, et al. (Tetrahedron Lett., 1986, 27, 6103-6106). Ethyl difluoroiodoacetate (0.355 mL, 651 mg, 2.60 mmol) was added to a rapidly stirred suspension of copper powder (333 mg, 5.24 mmol) in DMSO (6.5 mL) at rt. After 50 min., 3-bromo-6-methylpyridazine (300 mg, 1.73 mmol) was added in DMSO (1.0 mL). After 20 h, the mixture was transferred to a separatory funnel containing water (25 mL) and saturated aq. NH4Cl (25 mL), and extracted with ethyl acetate (2×50 mL). The organic extracts were washed with saturated aq. brine, dried (sodium sulfate), decanted, and evaporated. Purification by flash column chromatography on silica gel, eluting with 70:30 v/v hexanes/ethyl acetate, gave 363 mg of the title compound as an amber liquid. For the title compound:

後処理

  1. waitAfter 20 h
  2. customthe mixture was transferred to a separatory funnel
  3. extractionextracted with ethyl acetate (2×50 mL)
  4. washThe organic extracts were washed with saturated aq. brine
  5. dry with materialdried (sodium sulfate)
  6. customdecanted
  7. customevaporated
  8. customPurification by flash column chromatography on silica gel
  9. washeluting with 70:30 v/v hexanes/ethyl acetate

出典と根拠

ORDレコード
ord-726048f0ccc44fd395df3e4a13334032
出典データセット
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06593346B2

反応ノート

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