HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763982Generated: October 26, 2026
Isobutylene → 1,1,1-Tribromo-4-methylpent-4-en-2-ol
https://huagongshe.com/reaction/1763982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | Tribromoacetaldehyde | HCID 8256 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,1,1-Tribromo-4-methylpent-4-en-2-ol | HCID 13238428 | 85% |
Reaction Steps
A mixture of 281 parts of tribromoacetaldehyde, 168 parts of isobutene and 150 parts of petroleum ether was cooled to - 20° to - 5° C., and 13 parts of anhydrous aluminum chloride was added to the mixture dividedly in several times. The mixture was agitated at the above temperature for 5 hours. As the reaction advanced, crystals were precipitated from the reaction mixture. At the point of termination of the reaction, diethyl ether was added to the reaction mixture to form a homogeneous solution. The solution was then agitated at room temperature for 30 minutes, and 200 parts of water was added to the reaction mixture. The organic layer was recovered, low-boiling-point substances were removed by distillation, and the residue was subjected to distillation under reduced pressure to obtain 287 parts of 1,1,1-tribromo-4-methyl-4-penten-2-ol. The yield was 85%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04113968 |
|---|
| Source dataset | uspto-grants-1978_09 |
|---|
| ORD ID | ord-ba4c70c5000843929bd6187776349431 |
|---|
| Source note | uspto-grants-1978_09 |
|---|