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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824485Generated: November 1, 2026

Pyrrolidine → Pyrrolidine, 1-(isocyanoacetyl)-

https://huagongshe.com/reaction/1824485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantMethyl isocyanoacetateHCID 547815—
ProductPyrrolidine, 1-(isocyanoacetyl)-HCID 645547696.1%

Reaction Steps

To a stirred and cooled (0° C.) methyl isocyanoacetate (technical grade, 95%; 5.00 g, 47.8 mmol) was slowly added pyrrolidine (6.5 ml, 78 mmol). The mixture was stirred overnight with continued cooling and then concentrated. The resulting oil was repeatedly coevaporated from methylene chloride/hexane to remove residual pyrrolidine. Crude product, which was used in the next step without further purification, was thus afforded as 6.35 g (96%) of dark brown oil: 1H NMR (CDCl3) δ 4.24 (s, 2H), 3.53 (t, J=6.8, 2H), 3.41 (t, J=6.8, 2H), 2.02 (quintet, J=6.8, 2H), 1.90 (quintet, J=6.8, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041831B2
Source datasetuspto-grants-2006_05
ORD IDord-ea2b138349734d248107b41f92a0b9f6
Source noteuspto-grants-2006_05