Hydrochloric Acid → HCID 68145829, compound

HRID 1415007Notes

Reaction equation

HRID 1415007 reaction equation
[CH2:1]([C@:3]12[CH2:11][CH2:10][C@@H:9]3[C:12]4[CH2:13][CH:14]=[C:15]([O:20]C)[CH2:16][C:17]=4[CH2:18][CH2:19][C@H:8]3[C@@H:7]1[CH2:6][CH2:5][C@@H:4]2[O:22][CH3:23])[CH3:2].CO.Cl>O1CCCC1.O>[CH2:1]([C@:3]12[CH2:11][CH2:10][C@@H:9]3[C@@H:12]4[C:17]([CH2:18][CH2:19][C@H:8]3[C@@H:7]1[CH2:6][CH2:5][C@@H:4]2[O:22][CH3:23])=[CH:16][C:15](=[O:20])[CH2:14][CH2:13]4)[CH3:2]

Participants

6

Procedure

Add 13β-ethyl-3, 17β-dimethoxy-gona-2,5(10)-diene (0.8 g.) in tetrahydrofuran (5 cc.) to methanol (72 cc.) in an atmosphere of nitrogen and add a mixture of hydrochloric acid (4.8 cc.) and water (3.2 cc.). Add a further 10 cc. of tetrahydrofuran and after 1 hour dilute the solution with water and extract with ether. Wash, dry and evaporate the ethereal extracts and chromatograph the residue on neutral alumina. Remove impurities by elution with benzene. Wash the column with ether, evaporate the eluate and recrystallize the residue from hexane to obtain the title compound (0.2 g.), m.p. 117-119°; ultraviolet absorption λ max. 240 mμ (ε15,800); infrared spectrum (KBr disc) 6.0, 6.2, 8.8, 9.05 μ.

Workup

  1. additionadd
  2. additionAdd a further 10 cc
  3. extractionextract with ether
  4. washWash
  5. customdry
  6. customevaporate the ethereal extracts and chromatograph the residue on neutral alumina
  7. washRemove impurities by elution with benzene
  8. washWash the column with ether
  9. customevaporate the eluate and
  10. customrecrystallize the residue from hexane

Sources & evidence

ORD record
ord-91b75c42ece44fe084f90917cd91b7a4
Source dataset
uspto-grants-1977_01
Patent number
US04002746

Reaction notes

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