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Hydrochloric Acid → 3,4-Bis(4-methoxyphenyl)hex-3-ene

HRID 28274
Notes
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Reaction equation

HRID 28274 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9](=O)[CH2:10][CH3:11])=[CH:5][CH:4]=1.Cl>O1CCCC1>[CH3:6][CH2:9]/[C:10](/[C:11]1[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:8][CH:7]=1)=[C:9](\[C:6]1[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1)/[CH2:11][CH3:10]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 313Hydrochloric AcidHCID 671444-Propanoylanisole

Product 1

HCID 30325393,4-Bis(4-methoxyphenyl)hex-3-eneYield 92.2%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

Zinc dust (654 mg, 10.0 mmol) was slurried in 20 ml dry tetrahydrofuran under an inert atmosphere, and a solution of titanium tetrachloride (0.55 ml, 5.0 mmol) in 3 ml dry benzene was added. The resulting mixture was refluxed overnight to form active Ti(II) reagent, and a solution of para-methoxypropiophenone (500 mg, 3.0 mmol) in 5 ml dry tetrahydrofuran was added. After refluxing for twelve hours, the solution was cooled to room temperature, poured into 50 ml 2 N aqueous hydrochloric acid, and extracted with ether. The ether extracts were combined, washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate, and concentrated by solvent removal at the rotary evaporator. The residue was purified by chromatography on silica gel to give 410 mg (91%) dimestrol identified by ir, nmr, and mass spectra; mp 124°.

Workup

  1. temperatureAfter refluxing for twelve hours
  2. extractionextracted with ether
  3. washwashed with saturated aqueous sodium chloride solution
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated by solvent removal at the rotary evaporator
  6. customThe residue was purified by chromatography on silica gel

Sources & evidence

ORD record
ord-5685acae4bf74a8e996b55dda6621556
Source dataset
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04225734

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes