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2-Iodobenzoic acid → (6S)-7-(4-fluorophenoxy)-6-hydroxyheptanal

HRID 413577
ノート
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反応式

HRID 413577 の反応式
[F:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][CH2:7][C@@H:8]([OH:15])[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][OH:14])=[CH:4][CH:3]=1.IC1C=CC=CC=1C(O)=O>C1COCC1.CS(C)=O>[F:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][CH2:7][C@@H:8]([OH:15])[CH2:9][CH2:10][CH2:11][CH2:12][CH:13]=[O:14])=[CH:16][CH:17]=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 2

HCID 69412-Iodobenzoic acidHCID 59971312(6S)-7-(4-fluorophenoxy)-heptane-1,6-diol

生成物 1

HCID 59064024(6S)-7-(4-fluorophenoxy)-6-hydroxyheptanal収率 61.9%

試薬・触媒・溶媒 2

HCID 679Dimethyl Sulfoxide溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of (6S)-7-(4-fluorophenoxy)-heptane-1,6-diol (3.6 g, 14.8 mmol) in dry THF (60 ml) was added dropwise a solution of 2-iodobenzoic acid (5 g, 17.8 mmol) in dry DMSO (4 ml) over a period of 25 minutes at room temperature. After 15 minutes the reaction mixture was decomposed with crushed ice, filtered through celite and concentrated. The residue was extracted with ethylether, washed with brine, dried over Na2SO4 and the organic solvent was removed under reduced pressure. The residue was purified by silica gel chromatography using EtOAc-hexane (1:9) to give (6S)-7-(4-fluorophenoxy)-6-hydroxy-heptanal (2.2 g, 61.6%); [α]D+12 (c 3.8, CHCl3), 1H-NMR (CDCl3, 200 Hz): δ 1.4-1.8 (m, 6H), 2.49 (dt, 2H), 3.71-4.05 (m, 4H), 6.782-4H), 9.8 (s, 1H); HRMS (FAB): calcd. for C13H17O3F (M+) 240.116173 found 240.116465.

後処理

  1. filtrationfiltered through celite
  2. concentrationconcentrated
  3. extractionThe residue was extracted with ethylether
  4. washwashed with brine
  5. dry with materialdried over Na2SO4
  6. customthe organic solvent was removed under reduced pressure
  7. customThe residue was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-3ac47820459b48d69650976dfd431b4a
出典データセット
uspto-grants-2003_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06566538B1

反応ノート

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