Formaldehyde → 5-Hydroxymethyl-4-(4-(methylsulfonyl)phenyl)-3-phenyl-2-(5H)-furanone

HRID 325191

反応式

HRID 325191 の反応式
[C:1]1([C:7]2[C:8](=[O:22])[O:9][CH2:10][C:11]=2[C:12]2[CH:17]=[CH:16][C:15]([S:18]([CH3:21])(=[O:20])=[O:19])=[CH:14][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:23]=[O:24].C1C[O:28][CH2:27]C1.[C:30]([O-])([O-])=[O:31].[K+].[K+]>O>[OH:28][CH2:27][CH:10]1[O:9][C:8](=[O:22])[C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)=[C:11]1[C:12]1[CH:17]=[CH:16][C:15]([S:18]([CH3:21])(=[O:20])=[O:19])=[CH:14][CH:13]=1.[OH:24][CH2:23][C:10]1([CH2:30][OH:31])[O:9][C:8](=[O:22])[C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)=[C:11]1[C:12]1[CH:17]=[CH:16][C:15]([S:18]([CH3:21])(=[O:20])=[O:19])=[CH:14][CH:13]=1

参加物

7

実験手順

A mixture of 3-phenyl-4-(4-(methylsulfonyl)phenyl)-2-(5H)-furanone from Step 1 (0.31 g, 1.0 mmol), 37% aqueous formaldehyde solution (0.1 mL), THF (20 mL) and water (5 mL) was treated with K2CO3 (20 mg, 0.15 mmol). After stirring for 1 h at room temperature, the reaction mixture was quenched with 15 mL of saturated aqueous NH4Cl and extracted with 50 mL of EtOAc. The extract was dried over MgSO4 and concentrated. The residue was purified by flash chromatography eluting with 3:1 EtOAc/hexanes to give 50 mg of the title compound along with 120 mg of 5,5-bis(hydroxymethyl)-3-phenyl-4-(4-(methylsulfonyl)phenyl)-2-(5H)-furanone.

後処理

  1. customthe reaction mixture was quenched with 15 mL of saturated aqueous NH4Cl
  2. extractionextracted with 50 mL of EtOAc
  3. dry with materialThe extract was dried over MgSO4
  4. concentrationconcentrated
  5. customThe residue was purified by flash chromatography
  6. washeluting with 3:1 EtOAc/hexanes

出典と根拠

ORDレコード
ord-c5a18eb3f1f343afb394a3a348a0ce3f
出典データセット
uspto-grants-2001_04
特許番号
US06222048B1

関連ノート

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