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Potassium Bromide → tert-butyl (3R)-3-formylpyrrolidine-1-carboxylate

HRID 1364990
ノート
印刷プレビュー

反応式

HRID 1364990 の反応式
[C:1]([N:8]1[CH2:12][CH2:11][C@@H:10]([CH2:13][OH:14])[CH2:9]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].CC1(C)N([O])C(C)(C)CCC1.[Br-].[K+].[O-]Cl.[Na+].C([O-])(O)=O.[Na+]>C(Cl)Cl.O>[C:4]([O:3][C:1]([N:8]1[CH2:12][CH2:11][C@@H:10]([CH:13]=[O:14])[CH2:9]1)=[O:2])([CH3:7])([CH3:6])[CH3:5]
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

8

反応物 5

HCID 253877Potassium BromideHCID 516892Sodium BicarbonateHCID 1514340tert-Butyl (3R)-3-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 2724126TempoHCID 23665760Sodium Hypochlorite

生成物 1

HCID 1514342tert-butyl (3R)-3-formylpyrrolidine-1-carboxylate収率 87%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6344Dichloromethane溶媒

反応条件

温度
5 °C

実験手順

To a solution of (R)-Boc-3-pyrrolidinemethanol (5.0 g, 24.8 mmol) in DCM was added TEMPO (80 mg, 0.5 mmol) and potassium bromide (150 mg, 1.3 mmol). This mixture was cooled to 5° C. and vigorously stirred as a pre-chilled (at 0° C.) 1:1 mixture of NaOCl in water (53 mL) and a saturated, aqueous NaHCO3 solution (53 mL) was added dropwise. The resultant mixture was extracted with DCM (3×50 mL). The combined organic layers were washed with water (50 mL) and saturated aqueous NaCl (50 mL). The organic layer was dried over anhydrous Na2SO4 to yield 4.3 g of the title compound, which was used without further purification.

後処理

  1. temperaturea pre-chilled
  2. extractionThe resultant mixture was extracted with DCM (3×50 mL)
  3. washThe combined organic layers were washed with water (50 mL) and saturated aqueous NaCl (50 mL)
  4. dry with materialThe organic layer was dried over anhydrous Na2SO4

出典と根拠

ORDレコード
ord-0c9c69f2b97d448091afe09b599d8c7b
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07888386B2

反応ノート

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