Triethylamine → HCID 54503705, compound

HRID 1415979Notes

Reaction equation

HRID 1415979 reaction equation
[CH2:1]1[O:17][C:4]2([CH:8]([OH:9])[CH2:7][C:6]3([CH2:14][CH2:13][C:12](=[O:15])[CH2:11][CH2:10]3)[N:5]2[CH3:16])[O:3][CH2:2]1.C(N(CC)CC)C.[CH3:25][S:26](Cl)(=[O:28])=[O:27]>C(Cl)Cl>[CH2:2]1[O:3][C:4]2([CH:8]([O:9][S:26]([CH3:25])(=[O:28])=[O:27])[CH2:7][C:6]3([CH2:10][CH2:11][C:12](=[O:15])[CH2:13][CH2:14]3)[N:5]2[CH3:16])[O:17][CH2:1]1

Participants

5

Procedure

To a mixture of 3-Hydroxy-1-methyl-1-azaspiro[4.5]decane-2,8-dione ethylene ketal (1.0 g), triethylamine (1.73 mL) and methylene chloride (10 mL) was added methanesulfonyl chloride (950 mg) dissolved in methylene chloride (5 mL) in a dropwise fashion at 0° C. After 30 min the reaction mixture was washed with water, the organic layer dried over magnesium sulfate and the solvent was removed in vacuo. The resulting residue was filtered through silica gel with ethyl acetate as the eluent to afford 3-Mesyloxy-1-methyl-1-azaspiro[4.5]decane-2,8-dione ethylene ketal as an oil.

Workup

  1. washAfter 30 min the reaction mixture was washed with water
  2. dry with materialthe organic layer dried over magnesium sulfate
  3. customthe solvent was removed in vacuo
  4. filtrationThe resulting residue was filtered through silica gel with ethyl acetate as the eluent

Sources & evidence

ORD record
ord-336ddadc5f9d4b448b807649950f6f61
Source dataset
uspto-grants-1999_06
Patent number
US05910590

Reaction notes

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