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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236503Generated: October 30, 2026

HCID 11436030, compound → HCID 59300343, compound

https://huagongshe.com/reaction/2236503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11436030HCID 11436030—
ReactantHCID 178455850HCID 178455850—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59300343HCID 5930034375.1%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-e9eae0d6a9f74e6586d2c6807db236c6
Source noteuspto-grants-2010_05