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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256560Generated: October 26, 2026

Pyrrole → N-Triisopropylsilylpyrrole

https://huagongshe.com/reaction/256560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrroleHCID 8027—
ReactantTriisopropylsilyl chlorideHCID 139400—
ReactantPotassium tert-butoxideHCID 23665647—
Catalyst18-Crown-6HCID 28557—
SolventDiethyl EtherHCID 3283—
ProductN-TriisopropylsilylpyrroleHCID 14513686%

Reaction Steps

Pyrrole (2.9 ml, 42 mmol) was added dropwise with stirring at room temperature to a suspension of potassium tert-butoxide (4.66 g, 42 mmol) and 18-crown-6 (0.2 g, 0.76 mmol) in ether (300 ml). After 1 hour tri-isopropylsilyl chloride (8.0 g, 42 mmol) was added dropwise, and then the reaction mixture was stirred for 16 hours, and filtered. The residue was washed with ether and the combined filtrate and washings were washed with brine, then dried and concentrated to give N-tri-isopropylsilylpyrrole (8.0 g, 86% yield) as a clear oil, 1H nmr: delta 1.04 (18H, d), 1.38 (3H, m), 6.22 (2H, m), 6.72 (2H, m) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258360
Source datasetuspto-grants-1993_11
ORD IDord-4259472c90d64fd08f48ef74c18a68d2
Source noteuspto-grants-1993_11