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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111605Generated: October 30, 2026

Water → HCID 22766917, compound

https://huagongshe.com/reaction/1111605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantOxalic AcidHCID 971—
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic acidHCID 6422—
ReactantBenzene dimethylsulfoxideHCID 18518713—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
ProductHCID 22766917HCID 22766917—

Reaction Steps

N,N-dicyclohexylcarbodiimide (17.36 g, 0.084 mole) is added to a cooled, stirred solution of the above primary alcohol (6.09 g, 0.028 mole) in 63 ml of dimethyl sulfoxide-benzene (2:1) containing trifluoroacetic acid (1.12 ml, 0.014 mole) and pyridine (2.24 ml, 0.028 mole). The reaction is stirred at room temperature under nitrogen for 5 hr. The reaction mixture is now diluted with 600 ml of ether, followed by the dropwise addition of a solution of oxalic acid (7.56 g) in 21 ml of methanol. After 30 minutes, water (600 ml) is added and the insoluble material is collected. The organic phase is washed with water (2X), 5% aqueous sodium bicarbonate (2X) and water (2X). After drying (MgSO4) the organic phase is evaporated to yield an oil. The oil is purified by chromatography on silica gel. Elution with 10% ether in benzene affords the title compound as eluate, nmr (CDCl3) δ1.59 (s, 3H), 2.84 (t, J = 5.5 cps, 2H), 4.15 (t, J = 5.5 cps, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04118394
Source datasetuspto-grants-1978_10
ORD IDord-8cbdc7c4aff74ec2be9110bff4a560ba
Source noteuspto-grants-1978_10