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Trimethylaluminum → tert-butyl(2R,5R)-5-{[tert-butyl(dimethyl)silyl]oxy}-2-vinylpiperidine-1-carboxylate

HRID 255354
ノート
印刷プレビュー

反応式

HRID 255354 の反応式
[CH3:1][Al](C)C.[Si:5]([O:12][C@H:13]1[CH2:18][N:17]([C:19]([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20])[C@@H:16]([CH:26]=O)[CH2:15][CH2:14]1)([C:8]([CH3:11])([CH3:10])[CH3:9])([CH3:7])[CH3:6]>C1COCC1.ICI.C(OCC)(=O)C.[Zn]>[Si:5]([O:12][C@H:13]1[CH2:18][N:17]([C:19]([O:21][C:22]([CH3:24])([CH3:25])[CH3:23])=[O:20])[C@@H:16]([CH:26]=[CH2:1])[CH2:15][CH2:14]1)([C:8]([CH3:11])([CH3:9])[CH3:10])([CH3:6])[CH3:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 2

HCID 16682925TrimethylaluminumHCID 86630428tert-butyl(2R,5R)-5-{[tert-butyl(dimethyl)silyl]oxy}-2-formylpiperidine-1-carboxylate2 回

生成物 1

HCID 66774108tert-butyl(2R,5R)-5-{[tert-butyl(dimethyl)silyl]oxy}-2-vinylpiperidine-1-carboxylate

試薬・触媒・溶媒 4

HCID 23994Zinc触媒HCID 6346Diiodomethane溶媒
HCID 8028
Tetrahydrofuran
溶媒
2 回
HCID 8857Ethyl Acetate溶媒

実験手順

To a suspension of zinc dust (12.2 g) in THF (200 mL) and diiodomethane (5 mL) at 0° C. was added trimethylaluminium (2M in hexanes, 6 mL). After the addition the reaction was carefully warmed to room temperature (exothermic reaction!). The reaction was then cooled with an ice bath and a solution of tert-butyl (2R,5R)-5-{[tert-butyl(dimethyl)silyl]oxy}-2-formylpiperidine-1-carboxylate (Intermediate 189, 6.84 g) in THF (40 mL) was added. After 6 hours it was warmed to room temperature, the reaction was diluted with ethyl acetate and slowly quenched with a saturated aqueous solution of NaHCO3. The organic phase was collected and washed with NaHCO3 and brine, dried (Na2SO4), filtered and concentrated. Chromatography on silica gel with a gradient of 0-100% methylene chloride in hexanes gave 3.96 g of product.

後処理

  1. additionAfter the addition the reaction
  2. custom(exothermic reaction!)
  3. temperatureThe reaction was then cooled with an ice bath
  4. temperatureAfter 6 hours it was warmed to room temperature
  5. customslowly quenched with a saturated aqueous solution of NaHCO3
  6. customThe organic phase was collected
  7. washwashed with NaHCO3 and brine
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-8f4993e38ca74a7f8f4e59fb514c3187
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07875715B2

反応ノート

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