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Ammonia → Oxendolone

HRID 1154783
Notes
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Reaction equation

HRID 1154783 reaction equation
[CH2:1]([C@H:3]1[CH2:8][C@H:7]2[C@H:9]3[C@H:18]([CH2:19][CH2:20][C@:5]2([CH3:6])[C@H:4]1[OH:23])[C:17]1[CH:16]=[CH:15][C:14]([O:21]C)=[CH:13][C:12]=1[CH2:11][CH2:10]3)[CH3:2].O1CCCC1.N.[Li]>C(O)(C)(C)C>[CH2:1]([C@H:3]1[CH2:8][C@H:7]2[C@H:9]3[C@H:18]([CH2:19][CH2:20][C@:5]2([CH3:6])[C@H:4]1[OH:23])[C@@H:17]1[C:12](=[CH:13][C:14](=[O:21])[CH2:15][CH2:16]1)[CH2:11][CH2:10]3)[CH3:2]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 222Ammonia2×HCID 8028TetrahydrofuranHCID 3028194LithiumHCID 1283164716beta-Ethyl-3-methoxy-1,3,5(10)-estratrien-17beta-ol

Product 1

HCID 443947Oxendolone

Reagents, catalysts & solvents 1

HCID 6386tert-Butanol
Solvent

Conditions

Temperature
50 °C

Procedure

A solution of 2.0 g. of 16β-ethyl-3-methoxy-1,3,5(10)-estratrien-17β-ol in 40 ml. of tetrahydrofuran and 4 ml. of tert.-butanol is added dropwise at -40° C. to 80 ml. of ammonia. After the incremental introduction of 1.2 g. of lithium, the mixture is stirred for 2 hours at -40° C.; then the ammonia is allowed to evaporate, the residue is poured into about 200 ml. of water, and the mixture is extracted with ethyl acetate. The crude product is taken up in 40 ml. of methanol and 4 ml. of 4 N hydrochloric acid and agitated for 15 minutes at 50° C. Thereafter, the mixture is poured into water and extracted with methylene chloride. After recrystallizing the crude product from ethyl acetate/ether, 1.7 g. of 16β-ethyl-17β-hydroxy-4-estren-3-one is produced, m.p. 150°-152° C.

Workup

  1. customto evaporate
  2. additionthe residue is poured into about 200 ml
  3. extractionof water, and the mixture is extracted with ethyl acetate
  4. additionThereafter, the mixture is poured into water
  5. extractionextracted with methylene chloride
  6. customAfter recrystallizing the crude product from ethyl acetate/ether, 1.7 g

Sources & evidence

ORD record
ord-a7e1eac35c894d3aabd07696fa222da2
Source dataset
uspto-grants-1981_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04298538

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes