ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Methyl chloroformate → methyl 3-(1E)(4-(2-(4-fluorophenyl)-3-hydroxyprop-1-en-1-yl)phenyl)acrylate

HRID 2098567
ノート
印刷プレビュー

反応式

HRID 2098567 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[CH:12][C:13]2[CH:18]=[CH:17][C:16](/[CH:19]=[CH:20]/[C:21]([O:23][CH3:24])=[O:22])=[CH:15][CH:14]=2)[C:9](O)=[O:10])=[CH:4][CH:3]=1.C(N(CC)CC)C.ClC(OC)=O.[BH4-].[Na+]>C1COCC1.C(OCC)(=O)C.CO>[F:1][C:2]1[CH:7]=[CH:6][C:5](/[C:8](/[CH2:9][OH:10])=[CH:12]\[C:13]2[CH:18]=[CH:17][C:16]([CH:19]=[CH:20][C:21]([O:23][CH3:24])=[O:22])=[CH:15][CH:14]=2)=[CH:4][CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 6586Methyl chloroformateHCID 8471TriethylamineHCID 4311764Sodium borohydrideHCID 68771470HCID 68771470、化合物

生成物 1

HCID 68768999methyl 3-(1E)(4-(2-(4-fluorophenyl)-3-hydroxyprop-1-en-1-yl)phenyl)acrylate収率 79%

試薬・触媒・溶媒 3

HCID 887
Methanol
溶媒
HCID 8028Tetrahydrofuran溶媒
HCID 8857Ethyl Acetate溶媒

反応条件

温度
5 °C

実験手順

To a suspension of 2-(4-fluorophenyl)-3-(4-(3-(E)-methoxy-3-oxoprop-1-en-1-yl)phenyl)acrylic acid (2 g, 6.1 mmol, prepared according to the procedure described in Example 1, step-II) in THF (10 mL), triethylamine was added (0.85 mL, 6.67 mmol) under constant stirring at 5° C. To this solution, methyl chloroformate (0.53 mL, 6.67 mmol) was added dropwise over a period of 30 minutes at 5° C. and stirred at the same temperature for 30 minutes. To this reaction mixture, sodium borohydride (0.9 g, 24.5 mmol) was added at one portion and methanol (5 mL) was added dropwise under stirring and the reaction mixture was stirred at 30° C. for 2 hours. After completion of the reaction, the reaction mixture was diluted with ethyl acetate (300 mL) and washed successively with water (2×100 mL) and brine (1×100 mL). The organic layer was dried over anhydrous Na2SO4 and concentrated to afford the crude compound, which was purified by column chromatography using 12% ethylacetate/hexanes as the eluent to afford a pure compound as a white solid (1.5 g, 79% yield).

後処理

  1. customprepared
  2. stirringstirred at the same temperature for 30 minutes
  3. additionwas added dropwise
  4. stirringunder stirring
  5. stirringthe reaction mixture was stirred at 30° C. for 2 hours
  6. customAfter completion of the reaction
  7. washwashed successively with water (2×100 mL) and brine (1×100 mL)
  8. dry with materialThe organic layer was dried over anhydrous Na2SO4
  9. concentrationconcentrated
  10. customto afford the crude compound, which
  11. customwas purified by column chromatography

出典と根拠

ORDレコード
ord-90413f23e3c6454bbe4fe84621edfca5
出典データセット
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08450525B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート