4H-1-Benzopyran-2-carboxylic acid, 4-oxo-, methyl ester → HCID 12536095、化合物

HRID 574122ノート

反応式

HRID 574122 の反応式
[O:1]=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[O:5][C:4]([C:12](OC)=[O:13])=[CH:3]1.[BH4-].[Na+]>CO>[OH:13][CH2:12][C:4]1[O:5][C:6]2[C:11]([C:2](=[O:1])[CH:3]=1)=[CH:10][CH:9]=[CH:8][CH:7]=2

参加物

4

実験手順

500 mg of methyl 4-oxo-4H-chromene-2-carboxylate were dissolved in 25 ml of anhydrous methanol at room temperature, and NaBH4 was thereafter added to the solution slowly, until the starting material was no longer detected by TLC (about 300 mg). The solvent was then evaporated and a mixture of 1.1 gram of NaH2PO4.2H2O in 30 ml of water was added to the resulting residue. The pH of the mixture was maintained between 5 and 9, so as to prevent decomposition of chromone. The aqueous solution was washed with chloroform (3×50 ml) and the combined organic extracts were dried over Na2SO4. The solvent was evaporated to give 2-(hydroxymethyl)-4H-chromen-4-one which was used without future purification.

後処理

  1. customThe solvent was then evaporated
  2. additiona mixture of 1.1 gram of NaH2PO4.2H2O in 30 ml of water
  3. additionwas added to the resulting residue
  4. temperatureThe pH of the mixture was maintained between 5 and 9
  5. washThe aqueous solution was washed with chloroform (3×50 ml)
  6. dry with materialthe combined organic extracts were dried over Na2SO4
  7. customThe solvent was evaporated

出典と根拠

ORDレコード
ord-cfc367471d9e424f9b8be84b6d252a78
出典データセット
uspto-grants-2015_05
特許番号
US09034872B2

反応ノート

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