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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487543Generated: October 31, 2026

Ethyl Acetate → HCID 58631154, compound

https://huagongshe.com/reaction/1487543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 2-chloro-2-(hydroxyimino)acetateHCID 6399471—
ReactantHCID 58631078HCID 58631078—
SolventDimethylformamideHCID 6228—
ProductHCID 58631154HCID 5863115431.6%

Reaction Steps

To an ethyl acetate (20 ml) solution of (4S,5R)-tert-butyl 5-(4-ethynylphenyl)-4-(fluoromethyl)-2,2-dimethyloxazolidine-3-carboxylate (1.35 g, 4.0 mmol) is added a dimethylformamide solution of (E)-ethyl 2-chloro-2-(hydroxyimino)-acetate (12.5 ml, 1.5 g, 2.5 equiv). Sodium hydrogen carbonate (3.5 g) is added to the solution and it is allowed to stir overnight at room temperature. The mixture is filtered and diluted with ethyl acetate (100 ml). After washing with water (4×25 ml) the organic phase is concentrated to give the crude product, which is purified on silica gel using a gradient of ethyl acetate in hexanes (0% to 20% ethyl acetate) to give the title compound (567 mg): 1H NMR (400 MHz, CDCl3) 1.43-1.56 (m, 14H) 1.62 (s, 3H) 1.74 (br. s., 3H) 4.50 (q, J=7.24 Hz, 3H) 5.20 (d, J=7.33 Hz, 1H) 6.96 (s, 1H) 7.60 (d, J=8.34 Hz, 2H) 7.86 (d, J=8.59 Hz, 2H), m/z (CI) 449 ([M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428528B2
Source datasetuspto-grants-2016_08
ORD IDord-fd6ba7d00fa74198a5134fe5cff34edc
Source noteuspto-grants-2016_08