HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236503Generated: October 30, 2026
HCID 11436030, compound → HCID 59300343, compound
https://huagongshe.com/reaction/2236503
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11436030 | HCID 11436030 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59300343 | HCID 59300343 | 75.1% |
Reaction Steps
Allyl-(4-bromo-benzylidene)-amine (1.13 g, 5.0 mmol) is dissolved in THF (15 mL) and the mixture is cooled to 0° C. with an ice bath. Allyl magnesium bromide (6.0 mL, 1.0 M in ethyl ether, 6.0 mmol) is added. The resulting mixture is stirred at 0° C. for 1 hour and warmed to room temperature followed by reaction quenching. EtOAc and water were added and the EtOAc layer is washed with brine and dried. After removal of EtOAc, the product (1.0 g, 75%) is obtained. MS (ESI): 266, 268 (M+1)+1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713994B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-e9eae0d6a9f74e6586d2c6807db236c6 |
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| Source note | uspto-grants-2010_05 |
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