Sulfuric Acid → HCID 10354452, compound

HRID 1768731Notes

Reaction equation

HRID 1768731 reaction equation
[C:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7](Cl)=[O:8])=[CH:5][CH:4]=1)#[N:2].[NH:12]1[CH2:19][CH2:18][CH2:17][C@H:13]1[C:14]([OH:16])=[O:15].S([O-])([O-])(=O)=O.C[N+](C)(C)C.C[N+](C)(C)C.S(=O)(=O)(O)O>ClCCl.C(=O)([O-])O.[Na+]>[C:1]([C:3]1[CH:11]=[CH:10][C:6]([C:7]([N:12]2[CH2:19][CH2:18][CH2:17][C@H:13]2[C:14]([OH:16])=[O:15])=[O:8])=[CH:5][CH:4]=1)#[N:2]

Participants

7

Procedure

4.97 g of 4-cyanobenzoyl chloride, 3.45 g of L-proline and 0.73 g of tetramethylammonium sulphate in 300 ml of dichloromethane and 150ml of 5% sodium hydrogen carbonate solution are stirred for 48 hours. The aqueous phase is acidified with 3N sulphuric acid and extracted with ethyl acetate. The ethyl acetate phase is washed with saturated sodium chloride solution, dried and evaporated. Chromatography of the residue on silica gel (RP-18) using water gives 3.70 g of 1-(p-cyanobenzoyl)-L-proline. M.p. 80°-85° C.

Workup

  1. extractionextracted with ethyl acetate
  2. washThe ethyl acetate phase is washed with saturated sodium chloride solution
  3. customdried
  4. customevaporated

Sources & evidence

ORD record
ord-930a087a7a3a49879620eab06a1ff120
Source dataset
uspto-grants-1995_01
Patent number
US05378712

Reaction notes

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