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Methanol → HCID 57867352、化合物

HRID 1516253
ノート
印刷プレビュー

反応式

HRID 1516253 の反応式
C([O:9][C@H:10]1[C@:14]([F:16])([CH3:15])[CH:13]([O:17][CH3:18])[O:12][C@@H:11]1[CH2:19][OH:20])(=O)C1C=CC=CC=1.CO>N>[F:16][C@@:14]1([CH3:15])[CH:13]([O:17][CH3:18])[O:12][C@H:11]([CH2:19][OH:20])[C@H:10]1[OH:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 887MethanolHCID 57867350HCID 57867350、化合物

生成物 1

HCID 57867352HCID 57867352、化合物収率 70%

試薬・触媒・溶媒 1

HCID 222Ammonia溶媒

実験手順

(2R,3R,4R)-4-fluoro-2-(hydroxymethyl)-5-methoxy-4-methyl-tetrahydrofuran-3-yl benzoate (about 18 g, 63.3 mmol) in methanolic ammonia solution (25% w/w, 360 ml) was stirred at room temperature for about 36 hours, completion of the reaction monitored by thin-layer chromatography and methanol was removed under reduced pressure. Water added to the reaction mixture and extracted with ethyl acetate, the organic layer was dried over sodium sulphate and concentrated under reduced pressure. Purification by silica gel column chromatography using 20% ethyl acetate: hexane eluded the title compound (8 g) as an off-white solid. Yield: 70%; 1H NMR (300 MHz, CDCl3): δ 4.79 (d, 1H, J=10.8 Hz), 4.01-3.97 (m, 2H), 3.85 (d, 1H,), 3.71-3.66 (m, 1H), 3.44 (s, 3H), 2.05 (brs, 1H, —OH), 2.02 (brs, 1H, —OH), 1.47 (d, 3H, J=23.4 Hz); Mass: [M+Na]+: 203 (100%); IR cm−: 3437, 3372, 3294, 2924, 1459, 1102, 1049, 1006, 821, 731.

後処理

  1. customwas removed under reduced pressure
  2. additionWater added to the reaction mixture
  3. extractionextracted with ethyl acetate
  4. dry with materialthe organic layer was dried over sodium sulphate
  5. concentrationconcentrated under reduced pressure
  6. customPurification by silica gel column chromatography

出典と根拠

ORDレコード
ord-be8a0612e03640ccb96f231ddfa1823d
出典データセット
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08227431B2

反応ノート

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