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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881890Generated: November 1, 2026

2,3-Dihydroxybutanedioic Acid → Ethyl [2-(1,3-dioxolan-2-yl)-1,3-thiazol-5-yl](hydroxy)acetate

https://huagongshe.com/reaction/1881890

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydroxybutanedioic AcidHCID 875—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl [2-(1,3-dioxolan-2-yl)-1,3-thiazol-5-yl](oxo)acetateHCID 59331559—
SolventTetrahydrofuranHCID 8028—
ProductEthyl [2-(1,3-dioxolan-2-yl)-1,3-thiazol-5-yl](hydroxy)acetateHCID 5933129980%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of sodium borohydride (6.18 g) and DL-tartaric acid (24.5 g) in tetrahydrofuran (250 mL) was stirred at 80° C. for 2 hr. The reaction mixture was cooled to 0° C., ethyl [2-(1,3-dioxolan-2-yl)-1,3-thiazol-5-yl](oxo)acetate (10.49 g) was added, and the mixture was stirred at room temperature for 2 days. The reaction mixture was slowly poured into ice (100 g), and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO9) and concentrated. The obtained residue was subjected to silica gel column chromatography, and the title compound (8.43 g, yield 80%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (4:1, volume ratio). MS: 260 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318746B2
Source datasetuspto-grants-2012_11
ORD IDord-c2844104650542ceadff28de21895c01
Source noteuspto-grants-2012_11