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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508536Generated: November 3, 2026

Allyl bromide → HCID 86602875, compound

https://huagongshe.com/reaction/508536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 86602876HCID 86602876—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86602875HCID 86602875—

Reaction Steps

Allyl bromide (52 μL, 0.6 mmol) and DBU (65 μL, 0.6 mmol) were added to a solution of N-ethylcarbamate-5-hydroxy-6-iodo-8-ethyl-1,2,3,3a,8,8a-hexahydroindeno[1,2-c]pyrrole (116 mg, 0.3 mmol) in CH2Cl2 (3 mL), and stirred 2 hours at room temperature. The reaction solution was diluted with H2O and filtered through an Extrelut column. The column was washed with CH2Cl2 and the filtrate was concentrated. The crude product was purified via silica plug eluting with Hexanes/EtOAc (3/1, v/v) to afford 50 mg (39%−two steps) of the subtitle compound. MS calculated for C18H221NO3+H: 428, observed: 428.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096520B2
Source datasetuspto-grants-2015_08
ORD IDord-2a931e75e1dc41a4a132602e03e9a711
Source noteuspto-grants-2015_08