HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (RS)-2-(2-buten-1-yl)-6-isobutoxy-1-indanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (RS)-2-(2-buten-1-yl)-6-hydroxy-1-indanone | HCID 54363126 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (RS)-2-(2-buten-1-yl)-6-isobutoxy-1-indanone | HCID 54374731 | 93% |
Reaction Steps
A solution of 4.74 g of (RS)-2-(2-buten-1-yl)-6-hydroxy-1-indanone, 5.18 ml of isobutyl bromide and 5.98 g of potassium carbonate in 40 ml of N,N-dimethylformamide was heated to 60° for 48 hours. After cooling, the solution was poured into 100 ml of water and extracted twice with 70 ml of ethyl acetate each time. The combined organic phases were washed once with 70 ml of water and once with 70 ml of saturated sodium chloride solution, dried over magnesium sulfate and the solution was concentrated in a vacuum. 5.2 g (93%) of (RS)-2-(2-buten-1-yl)-6-isobutoxy-1-indanone were obtained as a red-brown oil which was used directly in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646173 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-638846c380fc4d65ae39cc7067e9c389 |
| Source note | uspto-grants-1997_07 |