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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566676Generated: October 25, 2026

Tetrahydrofuran → N-Methoxy-N-methylcyclopropanecarboxamide

https://huagongshe.com/reaction/566676

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantN-tert-butoxycarbonyl-3-methoxy-2-methylanilineHCID 10609918—
Reactant[2-(Tert-butoxycarbonylamino)-6-methoxyphenyl]methyl cyclopropyl ketoneHCID 10804518—
ReactantCID 53628100HCID 178418400—
SolventCyclohexaneHCID 8078—
ProductN-Methoxy-N-methylcyclopropanecarboxamideHCID 15643267—

Reaction Steps

Using the procedure described in Example 9, Part A, 100 mL (130 mmol) of 1.3M sec-butyl lithium in cyclohexane was reacted with N-tert-butoxycarbonyl-3-methoxy-2-methylaniline (15.4 g, 65 mmol) in 100 mL of THF and then with 8.4 g (65 mmol) of N-methoxy-N-methylcyclopropylcarboxamide to give crude [2-(tert-butoxycarbonylamino)-6-methoxyphenyl]methyl cyclopropyl ketone. This material on treatment with 20 mL of trifluoroacetic acid in 300 mL of methylene chloride for 6 hours gave a material that was chromatographed on silica gel. Eluting with a gradient, toluene→5% EtOAc/toluene, there was obtained 6.4 g (52% yield) of 2-cyclopropyl-4-methoxy-1H-indole as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06175021B1
Source datasetuspto-grants-2001_01
ORD IDord-97dbb582108d4f42affc744d6862dd3f
Source noteuspto-grants-2001_01