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4-(Benzyloxy)-3-methoxybenzaldehyde → (E)-4-[3-Methoxy-4-(phenylmethoxy)phenyl]-3-buten-1-ol

HRID 1721961
ノート
印刷プレビュー

反応式

HRID 1721961 の反応式
C([Li])CCC.[Br-].[OH:7][CH2:8][CH2:9][CH2:10][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[CH3:30][O:31][C:32]1[CH:33]=[C:34]([CH:37]=[CH:38][C:39]=1[O:40][CH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)[CH:35]=O>C1COCC1>[CH3:30][O:31][C:32]1[CH:33]=[C:34](/[CH:35]=[CH:10]/[CH2:9][CH2:8][OH:7])[CH:37]=[CH:38][C:39]=1[O:40][CH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=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 755064-(Benzyloxy)-3-methoxybenzaldehydeHCID 11025793(3-Hydroxypropyl)triphenylphosphonium bromideHCID 178418339Butyllithium

生成物 1

HCID 19862737(E)-4-[3-Methoxy-4-(phenylmethoxy)phenyl]-3-buten-1-ol収率 34%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

n-Butyllithium (1.55M in hexane, 194 ml) was added dropwise to a stirred suspension of (3-hydroxypropyl)triphenylphosphonium bromide (60.3 g) in dry THF (375 ml) cooled to 0° under nitrogen. The resulting blood-red solution was stirred at 0° for 15 min and then a solution of 3-methoxy-4-(phenylmethoxy)benzaldehyde (36.3 g) in dry THF (50 ml) was added dropwise over 15 min. The mixture was stirred at 0° for 30 min, allowed to warm up to room temperature, stirred for a further 2 h and then the reaction quenched by the addition of 2N hydrochloric acid (100 ml). The THF was removed in vacuo at 40°, the aqueous residue extracted with ethyl acetate (350 ml) and the organic layer washed with 2N HCl (200 ml). The aqueous phase was extracted with further ethyl acetate (150 ml), the organic layers combined, washed with 8% sodium bicarbonate solution (200 ml) and dried. Concentration afforded a product which was purified by FCC eluting with System B (1:2) yielding the title compound as a cream powder (14.5 g) m.p. 57°-61°

後処理

  1. temperaturecooled to 0° under nitrogen
  2. stirringThe mixture was stirred at 0° for 30 min
  3. stirringstirred for a further 2 h
  4. customthe reaction quenched by the addition of 2N hydrochloric acid (100 ml)
  5. customThe THF was removed in vacuo at 40°
  6. extractionthe aqueous residue extracted with ethyl acetate (350 ml)
  7. washthe organic layer washed with 2N HCl (200 ml)
  8. extractionThe aqueous phase was extracted with further ethyl acetate (150 ml)
  9. washwashed with 8% sodium bicarbonate solution (200 ml)
  10. customdried
  11. concentrationConcentration
  12. customafforded a product which
  13. customwas purified by FCC
  14. washeluting with System B (1:2)

出典と根拠

ORDレコード
ord-aa63562e998247d29e2b740e6a9d1769
出典データセット
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04853381

反応ノート

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