Potassium Carbonate → Diethyl 4-[[[5-(4-acetyl-3-hydroxy-2-propylphenoxy)pentyl]thio]methyl]-1,3-dithiolane-2,2-dipropanoate

HRID 1383149Notes

Reaction equation

HRID 1383149 reaction equation
[CH2:1]([O:3][C:4](=[O:21])[CH2:5][CH2:6][C:7]1([CH2:14][CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])[S:11][CH:10]([CH2:12][SH:13])[CH2:9][S:8]1)[CH3:2].[CH2:22]([C:25]1[C:37]([OH:38])=[C:36]([C:39](=[O:41])[CH3:40])[CH:35]=[CH:34][C:26]=1[O:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32]Br)[CH2:23][CH3:24].C(=O)([O-])[O-].[K+].[K+]>C(C(C)=O)C>[C:39]([C:36]1[CH:35]=[CH:34][C:26]([O:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][S:13][CH2:12][CH:10]2[CH2:9][S:8][C:7]([CH2:14][CH2:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])([CH2:6][CH2:5][C:4]([O:3][CH2:1][CH3:2])=[O:21])[S:11]2)=[C:25]([CH2:22][CH2:23][CH3:24])[C:37]=1[OH:38])(=[O:41])[CH3:40]

Participants

5

Procedure

The title compound was prepared according to the procedure of Example 2 using the mercaptan produced in Example 31 (0.5 g, 0.0014 mol), 5-(2-n-propyl-3-hydroxy-4-acetylphenoxy)-1-bromopentane (described in U.S. Pat. No. 4,565,882, Example 1) (0.484 g, 0.0014 mol) and anhydrous potassium carbonate (0.70 g) in methyl ethyl ketone (5 ml). The crude product was chromatographed on silica gel using 30% ethyl acetate/hexane as eluent to give 0.52 g (75%) of the product as an oil.

Workup

  1. customThe crude product was chromatographed on silica gel using 30% ethyl acetate/hexane as eluent

Sources & evidence

ORD record
ord-98bf17c0a30a49d3803fd32e326317f3
Source dataset
uspto-grants-1989_02
Patent number
US04808729

Reaction notes

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