Hydrochloric Acid → HCID 12942114, compound

HRID 848234Notes

Reaction equation

HRID 848234 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH:23][C:24](=[O:28])[N:25]([CH3:27])[CH3:26])[CH:5]=[CH:6][C:7]=1[O:8][CH2:9][CH2:10][CH2:11][C:12]1([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)OCC[O:13]1.O1CCCC1.Cl>[Cl-].[Na+].O>[C:12]([CH2:11][CH2:10][CH2:9][O:8][C:7]1[CH:6]=[CH:5][C:4]([NH:23][C:24](=[O:28])[N:25]([CH3:27])[CH3:26])=[CH:3][C:2]=1[Cl:1])(=[O:13])[C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1

Participants

5

Procedure

A mixture of 3-{3-chloro-4-[3-(2-phenyl-1,3-dioxolan-2-yl)propoxy]phenyl}-1,1-dimethylurea (2.03 g; 0.005 mol), tetrahydrofuran (10 ml) and 10% aqueous hydrochloric acid (2 ml) is stirred overnight. The reaction mixture is poured into brine (100 ml) and extracted with methylene chloride. The organic layer is washed with water, dried and evaporated to afford the product: 1.69 g of an off-white solid. Recrystallization from a toluene-hexane mixture (50 ml) yields 1.33 g of cream colored needles, m.p. 129°-130° C.

Workup

  1. extractionextracted with methylene chloride
  2. washThe organic layer is washed with water
  3. customdried
  4. customevaporated
  5. customto afford the product
  6. customRecrystallization from a toluene-hexane mixture (50 ml)
  7. customyields 1.33 g of cream colored needles, m.p. 129°-130° C.

Sources & evidence

ORD record
ord-1c830e65fe2348868fcc6875ef511b3c
Source dataset
uspto-grants-1981_10
Patent number
US04294986

Reaction notes

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