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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 560142Generated: October 25, 2026

N-bromobutanimide → 2-Bromo-3-ethoxycyclopent-2-enone

https://huagongshe.com/reaction/560142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-Ethoxycyclopent-2-en-1-oneHCID 89777—
SolventCarbon TetrachlorideHCID 5943—
Product2-Bromo-3-ethoxycyclopent-2-enoneHCID 10726911—

Reaction Steps

3-Ethoxy-cyclopent-2-enone (Intermediate NINE1) (commercially available from Aldrich) (10.0 g, 77.6 mmol) in carbon tetrachloride (15 mL) at 0° C. was treated with NBS (15.3 g, ˜85 mmol) added portion-wise over 30 m. After 1 h at 0° C. the mixture was partitioned between CH2Cl2 and saturated NaHCO3. The aqueous layer was extracted with CH2Cl2. The pooled organic layers were washed with H2O (2×) and dried over MgSO4. The mixture was filtered and evaporated to dryness. The solid was recrystallized from pentane:ether to give 13.3 g of 2-bromo-3-ethoxy-cyclopent-2-enone (Intermediate NINE2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063086B2
Source datasetuspto-grants-2011_11
ORD IDord-c1af453f698c43b0be8866a0cd8155a5
Source noteuspto-grants-2011_11