HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 389880, compound → HCID 10516051, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 389880 | HCID 389880 | — |
| Reactant | Triphenylmethyl phosphonium bromide | HCID 21951224 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10516051 | HCID 10516051 | 89.1% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a THF suspension (4.2 ml) containing triphenylmethylphosphonium bromide (0.536 g, 1.5 mmol) was added dropwise at 0° C. butyl lithium (1.4 mmol in 0.88 ml of 1.6M hexane solution). The reaction liquid was stirred at 0° C. for 30 minutes and then given 5,5-dicarboethoxy-7-octen-2-on (0.27 g, 1.0 mmol), followed by stirring at 0° C. for 1 hour. After treatment and purification as in Referential Example 9, there was obtained 0.239 g of diethyl allyl(3-methyl-3-butenyl)malonate (yields: 89%). Characteristic Values of allyl(3-methyl-3-butenyl)malonate
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06867161B1 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-f6e0f2e3342946799c5b503b9119ba60 |
| Source note | uspto-grants-2005_03 |