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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955277Generated: November 1, 2026

(+-)-3-Quinuclidinol → HCID 23294910, compound

https://huagongshe.com/reaction/1955277

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-3-QuinuclidinolHCID 15381—
ReactantCyclobutanecarbonyl chloride, 1-(3-nitrophenyl)-HCID 23294949—
SolventDichloromethaneHCID 6344—
ProductHCID 23294910HCID 23294910—

Reaction Steps

The title compound was prepared in an analogous manner to that in Example 36. 1-(3-Nitrophenyl)cyclobutanecarbonyl chloride, prepared from the compound prepared in Example 33, was reacted with 3-quinuclidinol in CH2Cl2 for 2 h. The crude was chromatographed on silica gel using EtOAc-Et3N 90:10 as eluent. The yield was 0.4 g (26%); mp 191-192° C.; 1H NMR (CD3OD) δ 1.73-2.29 (m, 7H), 2.62 (m, 2H), 2.94 (m, 2H), 3.02-3.36 (m, 5H), 3.65-3.75 (m, 1H), 5.10 (m, 1H), 7.60-7.66 (m, 1H), 7.74-7.78 (m, 1H), 8.13-8.18 (m, 2H). Anal. (C18H22N2O4.HCl) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124354
Source datasetuspto-grants-2000_09
ORD IDord-cce5c2187c344f2da17bd82739fdcee3
Source noteuspto-grants-2000_09