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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353238Generated: October 31, 2026

Pyridine → HCID 10920996, compound

https://huagongshe.com/reaction/353238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantO-ToluidineHCID 7242—
ReactantTetrahydrofuranHCID 8028—
ReactantValeryl chlorideHCID 61186—
SolventWaterHCID 962—
ProductHCID 10920996HCID 1092099684%

Reaction Steps

o-Toluidine (55 g) was mixed with 100 ml dry pyridine and 200 ml dry tetrahydrofuran in a 1-L 3-necked round bottom flask fitted with a Trubore stirrer, thermometer and a dropping funnel, under nitrogen. Then, with cooling in a refrigerated bath, valeryl chloride (60.3 g) was added dropwise over 1 hour. The mixture was stirred for another hour at room temperature and then poured onto 500 g ice and water. The precipitate was washed repeatedly with water on a Buchner funnel. The precipitate (88.9 g, 93%) was cyclized according to Verley and Bedure, 1925, Bull. Soc. Chim. Fr. (37): 190 to afford 2-n-butyl indole (67.4 g, 84%) as a very slightly yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750240B2
Source datasetuspto-grants-2004_06
ORD IDord-cd852605297a469e8990045675d30ee7
Source noteuspto-grants-2004_06