Sulfamic Acid → 3-Cyclopentyloxy-4-benzyloxybenzoic acid

HRID 1870384Notes

Reaction equation

HRID 1870384 reaction equation
[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

Participants

6

Procedure

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 warning 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 (10 g).

Workup

  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. customAfter warning 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

Sources & evidence

ORD record
ord-82cb65763d93493b96048ee60ffeb272
Source dataset
uspto-grants-2000_08
Patent number
US06096768

Reaction notes

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