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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236504Generated: October 30, 2026

HCID 59300355, compound → HCID 59299825, compound

https://huagongshe.com/reaction/2236504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59300355HCID 59300355—
CatalystHCID 178479819HCID 178479819—
SolventDichloromethaneHCID 6344—
ProductHCID 59299825HCID 5929982575%

Reaction Steps

Allyl-[1-(4-bromo-phenyl)-but-3-enyl]-carbamic acid tert-butyl ester (300 mg, 0.82 mmol) in CH2Cl2 (10 mL) is degassed and the 2nd generation of Grubb's catalyst (40 mg, 5%) is added under N2. The reaction did not proceed at room temperature and the mixture is brought to reflux. TLC is used to determine complete reaction of the olefin. The mixture is loaded onto a column and purified to provide the desired product (208 mg, 75%). 1H NMR (300 MHz, CDCl3) ∂7.43(2H, d, J=8.1 Hz), 7.17-7.26 (2H, m), 5.89-5.95 (1H, m), 5.34-5.58 (2H, m), 4.14-4.36 (1H, m), 3.35-3.44 (1H, m), 2.73-2.81 (1H, m), 2.41-2.62 (1H, m), 1.48 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-a9346d22013a40f994f7981008c7f47c
Source noteuspto-grants-2010_05