Phosgene → HCID 15042229, compound

HRID 1886575Notes

Reaction equation

HRID 1886575 reaction equation
[C:1]([Cl:4])(Cl)=[O:2].C(=O)([O-])[O-].[K+].[K+].[Cl:11][C:12]1[CH:35]=[CH:34][C:15]([O:16][CH:17]2[CH2:20][N:19](C(C3C=CC=CC=3)C3C=CC=CC=3)[CH2:18]2)=[CH:14][CH:13]=1>C(Cl)Cl>[Cl:11][C:12]1[CH:35]=[CH:34][C:15]([O:16][CH:17]2[CH2:18][N:19]([C:1]([Cl:4])=[O:2])[CH2:20]2)=[CH:14][CH:13]=1

Participants

5

Procedure

A solution of 32.34 g (0.33 mole) of phosgene in 200 ml of methylene chloride cooled with a tap water bath was treated with 45.5 g (0.33 mole) of potassium carbonate and stirred for 30 min, then 105 g (0.3 mole) of 3-(4-chlorophenoxy)-1-diphenylmethylazetidine in 600 ml of methylene chloride was added dropwise. After stirring for an additional 18 hr, the reaction mixture was filtered to remove the inorganic salts then concentrated in vacuo to a dark oily residue, 127.7 g. A solid formed upon standing which was triturated with boiling 30/60 petroleum ether 3 times to remove diphenylmethyl chloride. The residue, 33 g of dark brown crystalline material, was mainly starting material. Upon standing, a white crystalline material separated from the petroleum ether triturates (4.4 g, m.p. 78°-80° C.). The triturates were concentrated in vacuo, yielding 31 g of pale yellow tacky crystals. Trituration of these crystals with isopropyl ether yielded 21.9 g (35.6%) of pale yellow crystalline product.

Workup

  1. stirringAfter stirring for an additional 18 hr
  2. filtrationthe reaction mixture was filtered
  3. customto remove the inorganic salts
  4. concentrationthen concentrated in vacuo to a dark oily residue, 127.7 g
  5. customA solid formed
  6. customwas triturated
  7. customto remove diphenylmethyl chloride
  8. customa white crystalline material separated from the petroleum ether
  9. concentrationThe triturates were concentrated in vacuo

Sources & evidence

ORD record
ord-33fa93bcfa434a09b7db745d70540d2f
Source dataset
uspto-grants-1992_09
Patent number
US05151418

Reaction notes

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