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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710071Generated: October 29, 2026

Ethyl Acetate → HCID 86706784, compound

https://huagongshe.com/reaction/710071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantChlorosuccinimideHCID 31398—
Reactant(S)-t-Butyl 2-((hydroxyimino)methyl)pyrrolidine-1-carboxylateHCID 86706742—
SolventWaterHCID 962—
ProductHCID 86706784HCID 86706784294.3%

Reaction Steps

To an AcOEt (270 ml) solution of the (S)-t-butyl 2-((hydroxyimino)methyl)pyrrolidine-1-carboxylate (32.0 g) obtained in Example 2-(1), NMP (43.1 ml) was added and after adding NCS (21.94 g) in three divided portions at 20- to 30-min intervals at 30 to 40° C., the resulting mixture was stirred at room temperature for 0.5 hour. The same reaction was carried out in a total of four runs using the same quantities. To the reaction mixture, water (400 ml) was added and the organic layer was separated. The separated organic layers were combined, washed with water (1.2 L×2), dried (MgSO4), filtered and concentrated to give a crude product (pale yellow solid, 174 g), which was washed with AcOEt/hexane (AcOEt/hexane=140 ml/840 ml) and dried to give the titled compound (109.3 g, colorless solid.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181229B2
Source datasetuspto-grants-2015_11
ORD IDord-370d1406e5b84bafb0eb077e08ecf455
Source noteuspto-grants-2015_11