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Water → (2S,3S)-2-[Cbz(methyl)amino]-3-methylpentanal

HRID 2282800
ノート
印刷プレビュー

反応式

HRID 2282800 の反応式
[OH:1][CH2:2][C@@H:3]([N:8]([CH3:19])[C:9](=[O:18])[O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C@@H:4]([CH3:7])[CH2:5][CH3:6].C(N(CC)CC)C.O.COC(C)(C)C>CS(C)=O>[CH3:19][N:8]([C@@H:3]([C@@H:4]([CH3:7])[CH2:5][CH3:6])[CH:2]=[O:1])[C:9](=[O:18])[O:10][CH2:11][C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=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

6

反応物 4

HCID 962WaterHCID 8471TriethylamineHCID 15413tert-Butyl methyl etherHCID 11777636(2S,3S)-2-[Cbz(methyl)amino]-3-methylpentan-1-ol

生成物 1

HCID 10378073(2S,3S)-2-[Cbz(methyl)amino]-3-methylpentanal収率 87%

試薬・触媒・溶媒 1

HCID 679Dimethyl Sulfoxide
溶媒

反応条件

温度
0 °C

実験手順

To a solution of #1 (8.27 g, 31.2 mmol, 1 eq.) in dimethyl sulfoxide (41.35 mL, 0.75 M), was added triethylamine (8.70 mL, 64.0 mmol, 2.05 eq.) and the mixture was cooled to 0° C. Sulfur trioxide pyridine complex (10.18 g, 63.96 mmol, 2.05 eq.) was then added portion-wise, while keeping the internal temperature below 8° C. The reaction was allowed to reach room temperature and was stirred for 18 hours. The reaction was poured into water (100 mL) and tert-butyl methyl ether (100 mL). The aqueous layer was back-extracted with tert-butyl methyl ether (50 mL) and the combined organic layers were washed with brine (100 mL), dried over magnesium sulfate, filtered, concentrated in vacuo and purified by silica gel chromatography (Gradient: 10% to 60% ethyl acetate in heptane) to provide #2 (7.14 g, 87%) as a colorless oil. 1H NMR (400 MHz, DMSO-d6), presumed to be a mixture of rotamers, characteristic signals: δ 9.61 (s, 1H), 7.26-7.42 (m, 5H), 5.01-5.13 (m, 2H), 4.04-4.12 (m, 1H), 2.86 and 2.82 (2 s, total 3H), 1.94-2.11 (br m, 1H), 1.26-1.42 (br m, 1H).

後処理

  1. additionSulfur trioxide pyridine complex (10.18 g, 63.96 mmol, 2.05 eq.) was then added portion-wise
  2. customthe internal temperature below 8° C
  3. customto reach room temperature
  4. extractionThe aqueous layer was back-extracted with tert-butyl methyl ether (50 mL)
  5. washthe combined organic layers were washed with brine (100 mL)
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. custompurified by silica gel chromatography (Gradient: 10% to 60% ethyl acetate in heptane)

出典と根拠

ORDレコード
ord-b41e6a2aae3d45cfa145616403223929
出典データセット
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09138486B2

反応ノート

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