HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265976Generated: November 1, 2026
Ammonium Hydroxide → HCID 18548217, compound
https://huagongshe.com/reaction/1265976
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 3-Methyl-3-phenylbutan-2-one | HCID 285462 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 18548217 | HCID 18548217 | — |
Reaction Steps
Into a 250 ml round bottomed flask equipped with magnetic stirring and a reflux condenser was placed 15 g (98 mmol) of POCl3, 30 g (145 mmol) of PCl5, and 19.9 g (123 mmol) of α,α-dimethylbenzyl methyl ketone. The reaction was heated in an oil bath to an external temperature of 110° C. Gas evolution ceased after one hour. The reaction was cooled and carefully poured onto ice and aqueous ammonium hydroxide. Extractive workup with diethyl ether gave a mixture of 1-(α,α-dimethylbenzyl)-1-chloroethylene and 1-(α,α-dimethylbenzyl)-1,1-dichloroethane. Vacuum distillation gave purified 1-(α,α-dimethylbenzyl)-1-chloroethylene bp (23 torr) 110-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06548448B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-7959b68aa9334450a96302ac69f4592c |
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| Source note | uspto-grants-2003_04 |
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