Methanesulfonic Acid → 1,3-Dioxane-4-acetamide, 6-(cyanomethyl)-2,2-dimethyl-N,N-diphenyl-, (4R-cis)-(9CI)

HRID 1721450Notes

Reaction equation

HRID 1721450 reaction equation
[C:1]([CH2:3][CH:4]([OH:24])[CH2:5][CH:6]([OH:23])[CH2:7][C:8]([N:10]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:9])#[N:2].CO[C:27](OC)([CH3:29])[CH3:28].CS(O)(=O)=O>CC(C)=O>[C:1]([CH2:3][C@H:4]1[O:24][C:27]([CH3:29])([CH3:28])[O:23][C@@H:6]([CH2:7][C:8]([N:10]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)=[O:9])[CH2:5]1)#[N:2]

Participants

5

Procedure

Crude R-(R*,R*)!-6-cyano-3,5-dihydroxy-N,N-diphenylhexanamide, approximately 0.18 mol, is dissolved in 2,2-dimethoxypropane (160 mL, 1.5 mol) and acetone (300 mL). Methanesulfonic acid (0.5 mL) is added, and the solution is stirred for 2 hours at room temperature. The reaction is quenched by the addition of aqueous sodium bicarbonate (800 mL) and ethyl acetate (500 mL). The ethyl acetate solution is concentrated by vacuum distillation to give 62.5 g of (4R-cis)-6-(cyanomethyl)-2,2-dimethyl-N,N-diphenyl-1,3-dioxane-4-acetamide as an off-white crystalline solid (mp 98°-100° C., uncorrected).

Workup

  1. customThe reaction is quenched by the addition of aqueous sodium bicarbonate (800 mL) and ethyl acetate (500 mL)
  2. concentrationThe ethyl acetate solution is concentrated by vacuum distillation

Sources & evidence

ORD record
ord-727ed4f4f0bc4ec596df7858fd15a342
Source dataset
uspto-grants-1996_04
Patent number
US05510488

Reaction notes

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