HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979537Generated: October 27, 2026
Bromopinacolone → 2-Butanone, 1-(4-chlorophenoxy)-3,3-dimethyl-
https://huagongshe.com/reaction/979537
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromopinacolone | HCID 21642 | — |
| Reactant | Sodium 4-chlorophenolate | HCID 23666363 | — |
| Product | 2-Butanone, 1-(4-chlorophenoxy)-3,3-dimethyl- | HCID 90518 | — |
Reaction Steps
226 g (1 mol) of 1-(4-chlorophenoxy)-3,3-dimethylbutan-2-one (obtained from sodium 4-chlorophenolate and α-bromopinacolone; in this respect, see German Patent Specification No. 2,201,063), together with 120 g (1.07 mols) of glycerol, 19 g (0.1 mol) of p-toluenesulphonic acid monohydrate and 30 ml of butanol, are dissolved in 1,000 ml of toluene, and the mixture is heated under reflux for 16 hours in a water separator. After the mixture has been cooled, the toluene phase is washed with 4 times 250 ml of water, dried over magnesium sulphate, filtered, and evaporated down in vacuo. 186 g (65.4% of theory) of 2-(t-butyl)-2-(4-chlorophenoxymethyl)-4-hydroxymethyl-1,3-dioxolane of boiling point b.p.0.1 : 161° C.-163° C. are obtained by distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04668700 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-2a0c6b3cd24e4fe1939d48e48541747a |
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| Source note | uspto-grants-1987_05 |
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