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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009230Generated: October 30, 2026

Allyl bromide → HCID 67305114, compound

https://huagongshe.com/reaction/1009230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHCID 67304495HCID 67304495—
CatalystSilver(II) oxideHCID 92152—
SolventDiethyl EtherHCID 3283—
ProductHCID 67305114HCID 6730511482.1%

Reaction Conditions

Temperature40 °C

Reaction Steps

58 μl (0.70 mmol) of allyl bromide are added to a mixture of 162 mg (0.70 mmol) of silver oxide and 200 mg (0.47 mmol) of methyl (S)-3-[3′-(3-heptyl-1-methylureido)biphenyl-4-yl]-2-hydroxypropanoate in 3 ml of diethyl ether. The reaction mixture is stirred at 40° C. for 24 hours. The mixture is filtered and then the solvents are evaporated. The residue is chromatographed on silica gel (heptane/ethyl acetate 80/20 up to 60/40). 180 mg of methyl (S)-2-allyloxy-3-[3′-(3-heptyl-1-methylureido)biphenyl-4-yl]propanoate are obtained in the form of an oil. Yield=82%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973063B2
Source datasetuspto-grants-2011_07
ORD IDord-444469678ffd4e8d9b05c1a3116e67fd
Source noteuspto-grants-2011_07