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1,1-Dibromoethane → Methyl 8-methyl-2,3-dihydro-1,4-benzodioxin-6-carboxylate

HRID 642835
ノート
印刷プレビュー

反応式

HRID 642835 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([CH3:13])[C:11]=1[OH:12])[C:5]([O:7][CH3:8])=[O:6].C([O-])([O-])=O.[K+].[K+].Br[CH:21](Br)[CH3:22]>C(#N)C>[CH3:13][C:10]1[C:11]2[O:12][CH2:21][CH2:22][O:1][C:2]=2[CH:3]=[C:4]([C:5]([O:7][CH3:8])=[O:6])[CH:9]=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 112011,1-DibromoethaneHCID 11430Potassium CarbonateHCID 68609716Methyl 3,4-dihydroxy-5-methylbenzoate

生成物 1

HCID 45122025Methyl 8-methyl-2,3-dihydro-1,4-benzodioxin-6-carboxylate

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

A mixture of 34.0 g (0.19 mol) methyl 3,4-dihydroxy-5-methyl-benzoate, 77.12 g (0.56 mol) K2CO3 and 32.1 mL (0.37 mol) dibromoethane in 500 mL acetonitrile was refluxed for 6 h. The solid was filtered off, washed with 100 mL acetonitrile and the filtrate was evaporated to dryness i.vac. The residue was combined with 500 mL water and 500 mL EtOAc, the phases were separated, the organic phase was dried and evaporated to dryness i. vac. The residue was combined with 120 mL DIPE, the precipitate was suction filtered, washed with 50 mL DIPE and dried.

後処理

  1. temperaturewas refluxed for 6 h
  2. filtrationThe solid was filtered off
  3. washwashed with 100 mL acetonitrile
  4. customthe filtrate was evaporated to dryness i.vac
  5. customthe phases were separated
  6. customthe organic phase was dried
  7. customevaporated to dryness i
  8. filtrationfiltered
  9. washwashed with 50 mL DIPE
  10. customdried

出典と根拠

ORDレコード
ord-a89cb0e2877f49738337f624419e08f9
出典データセット
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07696195B2

反応ノート

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