Sodium Chloride → HCID 15351969, compound

HRID 992912Notes

Reaction equation

HRID 992912 reaction equation
[Cl:1]N1C(=O)CCC1=O.[C:9]1([CH2:15][O:16][C:17]2[CH:22]=[CH:21][C:20]([C@H:23]3[CH2:40][C@@:38]4([CH3:39])[C@@H:34]([CH2:35][CH2:36][C:37]4=[O:41])[C@H:33]4[C:24]3=[C:25]3[C:30]([CH2:31][CH2:32]4)=[CH:29][C:28](=[O:42])[CH2:27][CH2:26]3)=[CH:19][CH:18]=2)[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.[Na+].[Cl-].C1CCCCC1>CN(C)C=O>[Cl:1][C:29]1[C:28](=[O:42])[CH2:27][CH2:26][C:25]2[C:30]=1[CH2:31][CH2:32][C@@H:33]1[C:24]=2[C@@H:23]([C:20]2[CH:19]=[CH:18][C:17]([O:16][CH2:15][C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=3)=[CH:22][CH:21]=2)[CH2:40][C@@:38]2([CH3:39])[C@H:34]1[CH2:35][CH2:36][C:37]2=[O:41]

Participants

6

Procedure

5.295 g of N-chlorosuccinimide is added at 60° C. under an inert atmosphere to a solution of 13.6 g of 11β-[4-(phenylmethoxy)phenyl]-estra-4,9-diene-3,17-dione in 120 ml of dimethylformamide, agitation is carried out for 10 minutes then the reaction medium is poured into a saturated aqueous solution of NaCl, followed by extraction, washing, drying and evaporating under reduced pressure until the crude product is obtained (m=19.128 g). A second trial is carried out, the crude products are collected and purified by chromatography eluting with an ethyl acetate-cyclohexane mixture 30/70. 23.28 g of expected pure product is obtained. (Rf ACOET/cyclohexane 30/70=0.19).

Workup

  1. extractionfollowed by extraction
  2. washwashing
  3. customdrying
  4. customevaporating under reduced pressure until the crude product
  5. customis obtained (m=19.128 g)
  6. customthe crude products are collected
  7. custompurified by chromatography
  8. washeluting with an ethyl acetate-cyclohexane mixture 30/70
  9. custom23.28 g of expected pure product is obtained

Sources & evidence

ORD record
ord-30d0fa67522c47c3acf6f9d9cae80b27
Source dataset
uspto-grants-2002_10
Patent number
US06472382B2

Reaction notes

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