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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412667Generated: November 2, 2026

Picolyl chloride → HCID 20432090, compound

https://huagongshe.com/reaction/2412667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPicolyl chlorideHCID 23393—
ReactantSodiumHCID 5360545—
ReactantHCID 13309739HCID 13309739—
SolventDimethylformamideHCID 6228—
ProductHCID 20432090HCID 20432090—

Reaction Steps

Freshly liberated 2-picolinyl chloride was secured by extracting a mixture of 1.48 g potassium carbonate and 1.64 g 2-picolinyl chloride in 10 ml water with methylene chloride. The extract was dried (MgSO4) and concentrated (rotary evaporator). To the residue was added 10 ml dry dimethylformamide and the remaining methylene chloride was removed by further evaporation. The resulting solution was then added to a mixture of 10 mmol of the sodium salt of tetrahydro-5-(hydroxymethyl)-2,5-dimethyl-2-furancarbonitrile as a mixture of cis-trans isomers in 10 ml dry dimethylformamide prepared as described in Embodiment 10 above. The reaction progress and workup also followed the procedure for Embodiment 10 with the exception that crude product was secured from both pentane and ether extraction of the ice-quenched mixture. The crude product, which consisted of both cis- and trans-isomers, was purified and isomerically separated by preparative hplc using a silica gel column and ethyl acetate:pentane (60:40) as eluent. The cis (Z)-isomer amounted to 0.69 g, bp not determined.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04493936
Source datasetuspto-grants-1985_01
ORD IDord-1e241f415f0046a7b30cb3d0fc1ed60c
Source noteuspto-grants-1985_01