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

Ethylene Glycol → 2-[3-(Naphthalene-1-sulfonylmethyl)-4-nitro-phenoxy]-ethanol

HRID 2240014
ノート
印刷プレビュー

反応式

HRID 2240014 の反応式
F[C:2]1[CH:3]=[CH:4][C:5]([N+:22]([O-:24])=[O:23])=[C:6]([CH2:8][S:9]([C:12]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14][CH:13]=2)(=[O:11])=[O:10])[CH:7]=1.[CH2:25]([OH:28])[CH2:26][OH:27].C1COCC1>CC(C)([O-])C.[K+]>[C:12]1([S:9]([CH2:8][C:6]2[CH:7]=[C:2]([CH:3]=[CH:4][C:5]=2[N+:22]([O-:24])=[O:23])[O:27][CH2:26][CH2:25][OH:28])(=[O:11])=[O:10])[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH:15]=[CH:14][CH:13]=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 174Ethylene GlycolHCID 8028TetrahydrofuranHCID 593041751-(5-Fluoro-2-nitrobenzylsulfonyl)naphthalene

生成物 1

HCID 588120652-[3-(Naphthalene-1-sulfonylmethyl)-4-nitro-phenoxy]-ethanol収率 87.3%

試薬・触媒・溶媒 1

HCID 23665647Potassium tert-butoxide溶媒

実験手順

A mixture of 1-(5-fluoro-2-nitro-phenylmethanesulfonyl)-naphthalene (14.6 g, 42.3 mmol) and ethylene glycol (35 mL, 630 mmol) in 1.0 N potassium tert-butoxide in THF (90 mL, 90 mmol) was refluxed under nitrogen for one hour. After cooling to ambient temperature, the reaction mixture was concentrated. Excess water was added to the residue, and the mixture was poured into ice/2N hydrochloric acid. It was extracted with ethyl acetate and washed with water and brine. It was then dried with anhydrous magnesium sulfate, filtered, concentrated and dried in vacuo at 80° C. for 25 minutes to yield 2-[3-(naphthalene-1-sulfonylmethyl)-4-nitro-phenoxy]-ethanol as a brown gum (14.3 g, 87.2%). Mass Spectrum (−EI, [M−H]−) m/z 386. 1HNMR (500 MHz, DMSO-d6): δ8.56-8.57 (m, 1H), 8.35 (d, 1H, J=8.24 Hz), 8.14-8.15 (m, 1H), 8.00-8.02 (m, 2H), 7.65-7.75 (m, 3H), 7.11-7.13 (m, 1H), 6.89 (d, 1H, J=2.90 Hz), 5.27 (s, 2H), 4.92 (t, 1H, J=5.49 Hz), 3.93-3.95 (m, 2H), 3.67 ppm (dd, 2H, J=9.91 Hz and 5.34 Hz). Elemental Analysis for C19H17NO6S.0.25 mol H2O: Calcd: C, 58.23; H, 4.50; N, 3.57; Found: C, 57.83; H, 4.25; N, 3.50.

後処理

  1. temperaturewas refluxed under nitrogen for one hour
  2. concentrationthe reaction mixture was concentrated
  3. additionExcess water was added to the residue
  4. additionthe mixture was poured into ice/2N hydrochloric acid
  5. extractionIt was extracted with ethyl acetate
  6. washwashed with water and brine
  7. dry with materialIt was then dried with anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customdried in vacuo at 80° C. for 25 minutes

出典と根拠

ORDレコード
ord-8f781d02efb34d74b08f42c649a8d2b0
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07723329B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート