Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 19848970 | HCID 19848970 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14125903 | HCID 14125903 | — |
Reaction Steps
82.6 g=0.3 mol of 1-bromo-3-chloropropyl 4-methylphenyl ketone were added in portions at 0°-5° C. with stirring and cooling to a solution of 102 g=1.5 mol of imidazole in 150 ml of dimethylformamide, and the mixture was stirred for 15 hours at room temperature. For work-up, the mixture was poured into 1.5 liters of ice water and extracted twice with 150 ml of methylene chloride in each case, and the organic phase was washed twice with 100 ml of 2N NaOH in each case, dried over sodium sulfate and filtered. The solution thus prepared of the corresponding compound of the formula VII was added dropwise at 20° C. with vigorous stirring and cooling to a mixture of 70 ml of 50% strength sodium hydroxide solution and 1.6 g of tetrabutylammonium bromide, and the mixture was stirred for 8 hours at 20° C. and worked up as specified in Example 1. The oily residue (66.5 g, 98% of theory) crystallized. A sample of this had the melting point: 88°-90° C. from methyl tert.butyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04870088 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-fa90dfd7a3f74c0c939da9775cd6d147 |
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| Source note | uspto-grants-1989_09 |
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