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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494538Generated: October 31, 2026

Water → HCID 10402625, compound

https://huagongshe.com/reaction/1494538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-ChlorobenzaldehydeHCID 11477—
ReactantHCID 10399369HCID 10399369—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
ProductHCID 10402625HCID 1040262557.2%

Reaction Steps

To a solution of 1.6M n-butyl lithium in n-hexane (16.5 ml) in toluene (20 ml) at -20° C. under nitrogen was added a solution of 2-bromo-6,7,8,9-tetrahydro-3-methyl -5H-cyclohepta[b]pyridine (6.0 g, 0.025 m) in toluene (30 ml). The reaction mixture was kept at -20° C. for 0.25 hours and then blown over into a cooled solution of 3-chlorobenzaldehyde (3.7 g) in toluene (30 ml) at -20° C., and allowed to warm to room temperature. Water was added and the separated organic phase extracted with 2N hydrochloric acid. This was basified with solid potassium carbonate and extracted with chloroform. The combined chloroform extracts were washed with water, dried (MgSO4) and evaporated. The solid was purified by passing through a short silica column, eluted with chloroform, then re-crystallised from diethyl ether to give the title compound (4.31 g) m.p. 123°-5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026854
Source datasetuspto-grants-1991_06
ORD IDord-609c9e234a30440a88dbe372fe4de07a
Source noteuspto-grants-1991_06