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Ethyl Acrylate → Ethyl (3-hydroxy-6-methylpyridin-2-yl)propenoate

HRID 1754
ノート
印刷プレビュー

反応式

HRID 1754 の反応式
[OH:1][C:2]1[C:3](I)=[N:4][C:5]([CH3:8])=[CH:6][CH:7]=1.C([O-])(=O)C.[K+].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[C:34]([O:38][CH2:39][CH3:40])(=[O:37])[CH:35]=[CH2:36]>CN(C=O)C.O.[Pd](Cl)Cl>[OH:1][C:2]1[C:3]([C:35](=[CH2:36])[C:34]([O:38][CH2:39][CH3:40])=[O:37])=[N:4][C:5]([CH3:8])=[CH:6][CH:7]=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

8

反応物 4

HCID 8821Ethyl AcrylateHCID 11776TriphenylphosphineHCID 899572-Iodo-6-methylpyridin-3-olHCID 517044Potassium Acetate

生成物 1

HCID 131720091Ethyl (3-hydroxy-6-methylpyridin-2-yl)propenoate

試薬・触媒・溶媒 3

HCID 24290Palladium Chloride触媒
HCID 962
Water
溶媒
HCID 6228Dimethylformamide溶媒

反応条件

温度
120 °C

実験手順

To a solution of 3-hydroxy-2-iodo-6-methylpyridine (1.175 g, 5.0 mmol) in DMF (9.5 ml) and water (0.5 ml) were added potassium acetate (1.23 g, 12.5 mmol), triphenylphosphine (105 mg, 0.40 mmol), palladium chloride (36 mg, 0.20 mmol) and ethyl acrylate (1.63 ml, 1.50 g, 15.0 mmol). The mixture was placed under nitrogen and heated at 120° C. for 1.5 h. The mixture was cooled, filtered from deposited palladium black, and added to water (100 ml). The product was extracted into ethyl acetate (3×30 ml). The combined extracts were washed with water (2×25 ml) and with brine (25 ml), then dried over sodium sulphate and evaporated. This left a tan solid, the product (951 mg, 91%). mp 192°-195° C. (dec)

後処理

  1. temperatureThe mixture was cooled
  2. filtrationfiltered
  3. additionadded to water (100 ml)
  4. extractionThe product was extracted into ethyl acetate (3×30 ml)
  5. washThe combined extracts were washed with water (2×25 ml) and with brine (25 ml)
  6. dry with materialdried over sodium sulphate
  7. customevaporated
  8. waitThis left a tan solid

出典と根拠

ORDレコード
ord-daea2679130c4e96a69efc91647c4537
出典データセット
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05726315

反応ノート

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