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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 5-Methylthiazolidine-2,4-dione | HCID 10844415 | — |
| Reactant | Heptane tetrahydrofuran benzene | HCID 86600160 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-(5-methyl-2,4-dioxothiazolidin-5-yl)acetate | HCID 86707725 | 39% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680090B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-64e413c246cd497db658313f536e6751 |
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| Source note | uspto-grants-2014_03 |
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