HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl Alcohol → HCID 21288544, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl Alcohol | HCID 7858 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Benzene, 1-(chloromethyl)-4-(1,1-dimethylethyl)- | HCID 88198 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Product | HCID 21288544 | HCID 21288544 | — |
Reaction Steps
88 g (1.1 mol) of 50% sodium hydroxide solution are treated with 4.6 g (0.016 mol) of tetrabutylammonium chloride. At a temperature of 35° C. there is added dropwise within about 20 minutes while stirring well a mixture of 182.5 g (1.0 mol) of p-tert-butylbenzyl chloride and 61.5 g (1.06 mol) of allyl alcohol. The temperature is held at <70° C., which is accomplished if necessary by slight cooling. The mixture is stirred well at 70° C. for a further 12 hours. After cooling, the reaction mixture is washed twice with dilute hydrochloric acid. 204 g of practically pure p-tert-butylbenzyl allyl ether are obtained. The substance can be used without distillation for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04749815 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-8b46b3848e504b9f8cd7969197762cfe |
| Source note | uspto-grants-1988_06 |