HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870478Generated: October 30, 2026
N,N-Diethylaniline → HCID 22992851, compound
https://huagongshe.com/reaction/1870478
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Diethylaniline | HCID 7061 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 1-Bromo-4-chlorobutane | HCID 81364 | — |
| Reactant | HCID 22992846 | HCID 22992846 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 22992851 | HCID 22992851 | 43% |
Reaction Steps
918 mg of 8-chloro-2,3,4,5-tetrahydro-1,4-benzoxazepine-3,5-dione was dissolved in 20 ml of acetone, 1.2 g (2 equivalents) of potassium carbonate and 819 mg (1.1 equivalents) of 1-bromo-4-chlorobutane were added, and the mixture heated and refluxed for 7 hours. The resultant mixture was allowed to cool, then filtered. The filtrate was condensed and the residue obtained was dissolved in 2 ml of phosphorus oxychloride. Further, 1.4 ml (2 equivalents) of N,N-diethylaniline was added and the mixture was stirred at 90° C. for 12 hours. The phosphorus oxychloride was distilled off and a 10% sodium hydroxide aqueous solution added under ice cooling. The mixture was extracted with methylene chloride, then was washed with a saturated aqueous solution of potassium bicarbonate and saturated saline and dried over anhydrous magnesium sulfate. The solvent was distilled off and the crude product obtained was purified by silica gel column chromatograph (hexane:ethyl acetate=6:1) to obtain 598 mg of the above-identified compound (yield 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06096884 |
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| Source dataset | uspto-grants-2000_08 |
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| ORD ID | ord-f00cb79a1e9c499692004f162fc11203 |
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| Source note | uspto-grants-2000_08 |
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