Water → 7alpha-(5-Chloropentyl)-3-hydroxy-estra-1,3,5(10)-trien-17-one

HRID 650352Notes

Reaction equation

HRID 650352 reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C@@H:7]1[CH2:24][C:23]2[C@H:18]([CH2:19][CH2:20][C:21](=[O:25])[CH:22]=2)[C@@H:17]2[C@@H:8]1[C@H:9]1[C@@:13]([CH2:15][CH2:16]2)([CH3:14])[C:12](=[O:26])[CH2:11][CH2:10]1.[Br-].[Li+].O.C(=O)(O)[O-].[Na+]>C(#N)C.[Cu]Br.C(OCC)(=O)C>[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][C@@H:7]1[CH2:24][C:23]2[CH:22]=[C:21]([OH:25])[CH:20]=[CH:19][C:18]=2[C@@H:17]2[C@@H:8]1[C@H:9]1[C@@:13]([CH2:15][CH2:16]2)([CH3:14])[C:12](=[O:26])[CH2:11][CH2:10]1

Participants

8

Reactant 4

HCID 962WaterHCID 82050Lithium BromideHCID 516892Sodium BicarbonateHCID 571565697alpha-(5-Chloropentyl)-estr-4-ene-3,17-dione

Product 1

HCID 229418087alpha-(5-Chloropentyl)-3-hydroxy-estra-1,3,5(10)-trien-17-oneYield 53%

Reagents, catalysts & solvents 3

HCID 24593copper(I) bromideCatalystHCID 6342AcetonitrileSolvent2×HCID 8857Ethyl AcetateSolvent

Procedure

18.96 g of 7α-(5-chloropentyl)-estr-4-ene-3,17-dione is dissolved in 350 ml of anhydrous acetonitrile and mixed under inert gas at 80° C. with a solution of 4.36 g of lithium bromide and 22.5 g of copper(I) bromide in 390 ml of anhydrous acetonitrile. It is stirred for 5 more minutes, the mixture is cooled in an ice bath and mixed with water and ethyl acetate. The organic phase is shaken out with saturated sodium bicarbonate solution, the aqueous phase with ethyl acetate, the combined organic phases with saturated common salt solution, dried with sodium sulfate and concentrated by evaporation in a vacuum. The raw yield of 19.1 g is chromatographed on silica gel in hexane and ethyl acetate, whereby 10.0 g of oily 7α-(5-chloropentyl)-3-hydroxy-estra-1,3,5(10)-trien-17-one is obtained, which can be crystallized from hexane/dichloromethane.

Workup

  1. temperaturethe mixture is cooled in an ice bath
  2. dry with materialthe aqueous phase with ethyl acetate, the combined organic phases with saturated common salt solution, dried with sodium sulfate
  3. concentrationconcentrated by evaporation in a vacuum
  4. customThe raw yield of 19.1 g is chromatographed on silica gel in hexane and ethyl acetate

Sources & evidence

ORD record
ord-be02c070916f4c7bbf6e3121cc0fb5bb
Source dataset
uspto-grants-2001_08
Patent number
US06271403B1

Reaction notes

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