HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983770Generated: October 30, 2026
Benzaldehyde → Diethyl 2-benzylpropanedioate
https://huagongshe.com/reaction/983770
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Catalyst | HCID 178460666 | HCID 178460666 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Diethyl 2-benzylpropanedioate | HCID 69090 | — |
Reaction Steps
To an ether solution (7.5 ml) containing tetraisopropoxytitanium (0.284 g, 1.0 mmol) and diethyl malonate (0.145 g, 0.5 mmol) was added dropwise at −50° C. 1.53 ml of 1.31M ether solution containing isopropylmagnesium chloride (2 mmol). Upon stirring at −40° C. for 1 hour, the reaction liquid turned from yellow into brown. The reaction liquid was stirred together with benzaldehyde (0.080 g, 0.75 mmol) at 0° C. for 1 hour. With 1N hydrochloric acid added, the reaction liquid was stirred at room temperature for 15 minutes. After treatment and purification as in Referential Example 1, there was obtained diethyl benzylmalonate in deallylated form (yields: 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06867161B1 |
|---|
| Source dataset | uspto-grants-2005_03 |
|---|
| ORD ID | ord-6aec2b690c5d4574bfff4efad2c15e7e |
|---|
| Source note | uspto-grants-2005_03 |
|---|