HCID 178521466, compound → HCID 178521465, compound

HRID 1285582Notes

Reaction equation

HRID 1285582 reaction equation
[CH2-]C(C)=O.[S:5]1[CH:9]=[CH:8][CH:7]=[C:6]1[C:10]1[N:11]=[C:12]([C:15]2[CH:26]=[CH:25][C:18]([O:19][CH2:20][CH:21]([OH:24])[CH2:22][OH:23])=[CH:17][CH:16]=2)[NH:13][CH:14]=1>Cl.CC(C)=O>[S:5]1[CH:9]=[CH:8][CH:7]=[C:6]1[C:10]1[N:11]=[C:12]([C:15]2[CH:16]=[CH:17][C:18]([O:19][CH2:20][CH:21]([OH:24])[CH2:22][OH:23])=[CH:25][CH:26]=2)[NH:13][CH:14]=1

Participants

4

Reactant 1

HCID 178521466HCID 178521466, compound

Product 1

HCID 178521465HCID 178521465, compoundYield 86.6%

Reagents, catalysts & solvents 2

HCID 180AcetoneSolventHCID 313Hydrochloric AcidSolvent

Procedure

A mixture of 3-[p-[4-(2-thienyl)-2-imidazolyl]phenoxy]-1,2-propanediol acetonide (14.15 g., 0.04 m) in 3N HCl (80 ml.) and acetone (80 ml.) is refluxed for 0.5 hours. Acetone is removed under reduced pressure and the aqueous mixture is rendered alkaline with K2CO3. The solid is collected and dried in a vacuum oven at 60° C. to yield (III) (10.38 g., 82%, m.p. 197°-200° C.).

Workup

  1. temperatureis refluxed for 0.5 hours
  2. customAcetone is removed under reduced pressure
  3. customThe solid is collected
  4. customdried in a vacuum oven at 60° C.

Sources & evidence

ORD record
ord-0763c78e51c942e5aeb487849f9ebdcb
Source dataset
uspto-grants-1986_01
Patent number
US04567276

Reaction notes

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