HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581069Generated: October 30, 2026
Potassium Carbonate → 1-[p-(N',N'-dimethylureido)-phenoxy]-2-hydroxy-3-isopropylaminopropane
https://huagongshe.com/reaction/1581069
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Urea, N'-(4-hydroxyphenyl)-N,N-dimethyl- | HCID 3014146 | — |
| Reactant | 3-Isopropylamino-2-hydroxy-1-chloropropane | HCID 12624612 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-[p-(N',N'-dimethylureido)-phenoxy]-2-hydroxy-3-isopropylaminopropane | HCID 12666320 | — |
Reaction Steps
A mixture of 20 g of p-(N',N'-dimethylureido)-phenol, 15 g of 3-isopropylamino-2-hydroxy-1-chloropropane, and 20 g of finely ground potassium carbonate in 250 ml of acetone is stirred at 50° for 5 hours. The solid part of the mixture is filtered off and the acetone solution is evaporated in a vacuum. The residue is dissolved in 100 ml of 2N hydrochloric acid, the undissolved part is filtered off and the remaining mixture is extracted with methylene chloride. The aqueous phase is rendered alkaline by adding 2N sodium hydroxide solution and is extracted with methylene chloride. After the evaporation of the solvent, 1-[p-(N',N'-dimethylureido)-phenoxy]-2-hydroxy-3-isopropylaminopropane is isolated which melts at 138°-139° after recrystallisation from benzene and has the formula ##SPC6##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03935259 |
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| Source dataset | uspto-grants-1976_01 |
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| ORD ID | ord-163c6c30691d48c2a5e9791940fc7bb3 |
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| Source note | uspto-grants-1976_01 |
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