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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1190829Generated: November 1, 2026

Methyl bromoacetate → Methyl 2-(5-methyl-2,4-dioxothiazolidin-5-yl)acetate

https://huagongshe.com/reaction/1190829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl bromoacetateHCID 60984—
ReactantLithium diisopropylamideHCID 2724682—
Reactant5-Methylthiazolidine-2,4-dioneHCID 10844415—
ReactantHeptane tetrahydrofuran benzeneHCID 86600160—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(5-methyl-2,4-dioxothiazolidin-5-yl)acetateHCID 8670772539%

Reaction Conditions

Temperature-40 °C

Reaction Steps

To a stirred solution of Compound 1d (300 mg, 2.3 mmol) in THF (20 mL) at −40° C. was added 2 M LDA in heptane/THF/benzene (2.4 mL, 4.8 mmol) dropwise. After 15 minutes, methyl 2-bromoacetate (0.30 mL, 3.2 mmol) was added and the reaction mixture stirred at −40° C. for 2 h then quenched by dropwise addition of AcOH (0.8 mL). The reaction mixture was diluted with EtOAc, and the organic portion washed with water (2×), brine (2×), dried (Na2SO4), filtered and concentrated under reduced pressure. The product was purified by silica gel chromatography eluting with 0-100% EtOAc/hexanes to afford Compound 1e (180 mg, 39%) as a clear oil. LCMS=1.06 min using analytical method (B), 225.9 (M+Na). 1H NMR (400 MHz, CDCl3) δ 3.75 (s, 3H), 3.24-2.84 (m, 2H), 1.81 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680090B2
Source datasetuspto-grants-2014_03
ORD IDord-64e413c246cd497db658313f536e6751
Source noteuspto-grants-2014_03