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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478754Generated: October 31, 2026

2-cyclopropyl-N-methoxy-N-methylacetamide → HCID 66714089, compound

https://huagongshe.com/reaction/1478754

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-cyclopropyl-N-methoxy-N-methylacetamideHCID 22473766—
ReactantHCID 178455850HCID 178455850—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66714089HCID 66714089—

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a solution of 2-cyclopropyl-N-methoxy-N-methylacetamide (C63) (48 g, 0.3 mol) in tetrahydrofuran (900 mL) was added a solution of allylmagnesium bromide (1.0 M in diethyl ether, 1.5 L, 1.5 mol) drop-wise at −60° C. The mixture was stirred at −60° C. for 1 hour, then was quenched with saturated aqueous ammonium chloride solution (120 mL). The reaction was extracted with dichloromethane (2×500 mL), and the organic layers were washed with saturated aqueous sodium chloride solution (500 mL), dried and concentrated in vacuo to give the product as a yellow oil, which was used directly in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403846B2
Source datasetuspto-grants-2016_08
ORD IDord-18cad1fca11546ce8c9d215e242737da
Source noteuspto-grants-2016_08