Sulfamic Acid → 3-Cyclopentyloxy-4-benzyloxybenzoic acid

HRID 1489717ノート

反応式

HRID 1489717 の反応式
[CH2:1]([O:8][C:9]1[CH:16]=[CH:15][C:12]([CH:13]=[O:14])=[CH:11][C:10]=1[O:17][CH:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(=O)(=O)([OH:25])N.Cl([O-])=O.[Na+]>C(O)(=O)C.O>[CH:18]1([O:17][C:10]2[CH:11]=[C:12]([CH:15]=[CH:16][C:9]=2[O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[C:13]([OH:25])=[O:14])[CH2:22][CH2:21][CH2:20][CH2:19]1

参加物

6

実験手順

A rapidly stirred solution of 4-benzyloxy-3-cyclopentyloxybenzaldehyde (10.5 g; that is prepared as described in Reference Example 37) in glacial acetic acid (100 mL) is treated with sulfamic acid (4.85 g) and stirred at room temperature for 10 minutes. The solution is then cooled in an ice bath and treated with a solution of sodium chlorite (4.2 g) in water (100 mL) during 15 minutes at 13°-15° C. During the addition a white precipitate forms and, because stirring becomes difficult, a further quantity of glacial acetic acid (60 mL) is added. After warming to room temperature, the solution is stirred for a further 6 hours and further quantities of sodium chlorite (1.6 g) and sulfamic acid (1.7 g) are added. The mixture is poured onto water and the resulting solid is filtered off and dried, to give 3-cyclopentyloxy-4-benzyloxybenzoic acid (10g).

後処理

  1. customthat is prepared
  2. temperatureThe solution is then cooled in an ice bath
  3. additionDuring the addition a white precipitate forms
  4. stirringbecause stirring
  5. temperatureAfter warming to room temperature
  6. stirringthe solution is stirred for a further 6 hours
  7. additionThe mixture is poured onto water
  8. filtrationthe resulting solid is filtered off
  9. customdried

出典と根拠

ORDレコード
ord-70d1dc2775d84781986a94f2c9b1f092
出典データセット
uspto-grants-1997_10
特許番号
US05679696

反応ノート

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