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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484971Generated: October 30, 2026

Sodium Acetate → 3-(5-Bromothiophen-2-yl)-3-oxopropyl acetate

https://huagongshe.com/reaction/1484971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant1-(5-Bromothiophen-2-yl)-3-chloropropan-1-oneHCID 12867664—
SolventAcetic AcidHCID 176—
Product3-(5-Bromothiophen-2-yl)-3-oxopropyl acetateHCID 58169420541.3%

Reaction Conditions

Temperature130 °C

Reaction Steps

To the mixture of 1-(5-bromothiophen-2-yl)-3-chloropropan-1-one (2.8 g, 1.6 mmol, 1.0 eq), NaOAc (4.5 g, 55.3 mmol, 5 eq) and KI (200 mg) in acetic acid (16 mL) was stirred at 130° C. for overnight. The mixture was extracted with CH2Cl2 (3×40 ml). The combined organic layers were washed (brine), dried (Na2SO4), filtered and concentrated to give yellow oil 3-(5-bromothiophen-2-yl)-3-oxopropyl acetate (2.4 g, 76.2%). LC-MS (m/z)=278.1 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422271B2
Source datasetuspto-grants-2016_08
ORD IDord-084a0d1d274749099e563b97ab63ee30
Source noteuspto-grants-2016_08