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Water → 17-Methylenestra-1,3,5(10)-trien-3-yl methyl ether

HRID 275683
Notes
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Reaction equation

HRID 275683 reaction equation
[CH2:1]=[C:2]1[CH2:7][CH2:6][C@H:5]2[C@H:8]3[C@H:17]([CH2:18][CH2:19][C@:3]12[CH3:4])[C:16]1[CH:15]=[CH:14][C:13]([OH:20])=[CH:12][C:11]=1[CH2:10][CH2:9]3.[C:21](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O.O>C(O)C>[CH3:21][O:20][C:13]1[CH:14]=[CH:15][C:16]2[C@@H:17]3[C@H:8]([C@H:5]4[C@@:3]([CH2:19][CH2:18]3)([CH3:4])[C:2](=[CH2:1])[CH2:7][CH2:6]4)[CH2:9][CH2:10][C:11]=2[CH:12]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 962WaterHCID 6497Dimethyl Sulfate2×HCID 11430Potassium CarbonateHCID 1445855217-Methylene-estra-1,3,5(10)-trien-3-ol

Product 1

HCID 1110880617-Methylenestra-1,3,5(10)-trien-3-yl methyl etherYield 69%

Reagents, catalysts & solvents 1

HCID 702
Ethanol
Solvent

Procedure

To a stirred suspension of 17-methylenestra-1,3,5(10)-trien-3-ol (5.37 g, 20.0 mmol) and potassium carbonate (50.82 g, 0.3678 mol) at reflux in 90% ethanol (500 mL) was added dimethyl sulfate (5.0 mL, 53 mmol). After ½ h reflux additional dimethyl sulfate (36 mL, 0.38 mol, in three 12 mL aliquots) was added over the period of 1 h. See FIG. 17. The reaction was refluxed a further hour, following which 360 mL of water were added and the mixture was placed in the refrigerator overnight. The resulting suspension was filtered and washed with 80 mL of 60% methanol+three 80 mL portions of 5% (w/w) sodium hydroxide+three 80 mL portions of water. The residue was recrystallized from aqueous methanol to give white crystals (3.88 g, 13.7 mmol, 69%), m.p. 59-62° C. TLC (20% ethyl acetate/hexanes on silica gel) showed product (Rf 0.63) with trace contaminants at Rf 0.37 and at the origin.

Workup

  1. additionwas added over the period of 1 h
  2. temperatureThe reaction was refluxed a further hour
  3. additionwere added
  4. customwas placed in the refrigerator overnight
  5. filtrationThe resulting suspension was filtered
  6. washwashed with 80 mL of 60% methanol+three 80 mL portions of 5% (w/w) sodium hydroxide+three 80 mL portions of water
  7. customThe residue was recrystallized from aqueous methanol

Sources & evidence

ORD record
ord-f4fbf156de71461ab9e52bf362c7bdfd
Source dataset
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06352980B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes