1,2-Dichloroethane → HCID 22840071, compound

HRID 861374Notes

Reaction equation

HRID 861374 reaction equation
[C:1]([OH:11])(=[O:10])[CH2:2][CH2:3][C:4]1[CH:9]=CC=CC=1.[CH:12]1[CH:13]=[CH:14][C:15]2N(O)N=N[C:16]=2[CH:17]=1.C[N:23]1CCO[CH2:25][CH2:24]1.[CH2:29](Cl)CCl.[Li+].[OH-]>C1COCC1.O.CC(N(C)C)=O>[CH2:24]([N:23]1[CH2:9][CH2:4][CH2:3][C@H:2]1[C:1]([OH:11])=[O:10])[CH2:25][CH2:29][C:16]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:17]=1

Participants

8

Procedure

Hydrocinnamic acid (1.63 g., 11 mmol) and L-proline-OMe HCl (2.19 g., 13.2 mmol) were dissolved in 110 ml. of dimethylacetamide (DMAc), followed by the addition of 2.19 g. (14.3 mmol) of HOBt and adjustment to pH 8 with N-methylmorpholine (NMM). Then EDC (3.16 g., 16.5 mmol) was added and the solution stirred for 20 hr., followed by concentration in vacuo and extractive workup with EtOAc to afford 2.97 g. of oily residue, which was purified by chromatography on silica gel to yield 2.68 g. of methyl ester. This intermediate was saponified in 100 ml. of 50:50 THF/H2O using 5.2 ml. of 2.17N LiOH for 3 hr., to give, after acidification with dil. KHSO4, removal of the volatile solvents in vacuo, and extractive workup with EtOAc, the title compound as a colorless oil.

Workup

  1. concentration, followed by concentration in vacuo and extractive workup with EtOAc
  2. customto afford 2.97 g
  3. customof oily residue, which was purified by chromatography on silica gel
  4. customto yield 2.68 g
  5. custom, to give
  6. customafter acidification with dil. KHSO4, removal of the volatile solvents in vacuo, and extractive workup with EtOAc

Sources & evidence

ORD record
ord-ba3d6a1a6f964c90b4158a6611a68a47
Source dataset
uspto-grants-1998_02
Patent number
US05714485

Reaction notes

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