Toluene → 7beta-Methyl-3-tetrahydropyranyloxy-estra-1,3,5(10)-trien-17-one

HRID 850842Notes

Reaction equation

HRID 850842 reaction equation
[OH:1][C:2]1[CH:19]=[CH:18][C:17]2[C@@H:16]3[C@H:7]([C@H:8]4[C@@:12]([CH2:14][CH2:15]3)([CH3:13])[C:11](=[O:20])[CH2:10][CH2:9]4)[C@@H:6]([CH3:21])[CH2:5][C:4]=2[CH:3]=1.C1(C)C=CC(S(O)(=O)=[O:29])=CC=1.[C:33]1(C)C=[CH:37][CH:36]=[CH:35][CH:34]=1>O1C=CCCC1.C(OCC)(=O)C>[CH3:21][C@H:6]1[CH2:5][C:4]2[CH:3]=[C:2]([O:1][CH:37]3[CH2:36][CH2:35][CH2:34][CH2:33][O:29]3)[CH:19]=[CH:18][C:17]=2[C@@H:16]2[C@@H:7]1[C@H:8]1[C@@:12]([CH2:14][CH2:15]2)([CH3:13])[C:11](=[O:20])[CH2:10][CH2:9]1

Participants

6

Procedure

A suspension of 1.2 g of 3-hydroxy-7β-methyl-estra -1,3,5(10)-trien-17-one in 12 ml of toluene and 1.2 ml of dihydropyran is stirred with 5.6 mg of para-toluenesulfonic acid for 2 hours at room temperature. Then, it is diluted with ethyl acetate, washed with sodium bicarbonate solution as well as with saturated sodium chloride solution, dried on sodium sulfate, concentrated by evaporation in a vacuum and chromatographed on silica gel with hexane/acetone. 1.22 g of 7β-methyl-3-tetrahydropyranyloxy-estra-1,3,5(10)-trien-17-one is obtained.

Workup

  1. washwashed with sodium bicarbonate solution as well as with saturated sodium chloride solution
  2. customdried on sodium sulfate
  3. concentrationconcentrated by evaporation in a vacuum
  4. customchromatographed on silica gel with hexane/acetone

Sources & evidence

ORD record
ord-27c1ce5ed6e6427f9215d23083d74476
Source dataset
uspto-grants-2000_01
Patent number
US06018062

Reaction notes

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