HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 57242164, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2,2,4-Trimethyl-1-cyclohexanecarbaldehyde | HCID 21263740 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 57242164 | HCID 57242164 | 80.8% |
Reaction Steps
2,2,4-Trimethyl-1-cyclohexanecarbaldehyde (11 g, 72 mmole) in ether (100 ml) was added dropwise with stirring to a Grignard compound prepared from Mg (2.3 g) and allylbromide (10 g) in ether and refluxed for 2 h. After cooling, the mixture was hydrolyzed with NH4Cl-solution, then distilled at a bath temperature of 150°/0.5 hPa, to obtain 11.3 g (80%) of the desired product as a 2:1 mixture of 2 isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06177400B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-f0f38d8eae4f4a478dc83ed23c8fc1bf |
| Source note | uspto-grants-2001_01 |