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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376584Generated: October 31, 2026

Oxalyl chloride → HCID 18780160, compound

https://huagongshe.com/reaction/376584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant5-(Methoxymethyl)oxolane-2-carboxylic acidHCID 18780016—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 18780160HCID 18780160—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of (2RS,5SR)-5-methoxymethyltetrahydrofuran-2-carboxylic acid (3.1g) in dichloromethane (50ml) was treated with oxalyl chloride (2.68ml) and dimethylformamide (1 drop). The mixture was stirred for 1h and heated to reflux for 10 mins. The solvent was evaporated and then dichloromethane was evaporated from the residue twice. The product was dissolved in dichloromethane (100ml) and the solution cooled in an ice bath. Diazomethane was then passed into the solution as described in Example 14(a). When the addition was complete the mixture was stirred at 0° C. for 0.5h and then hydrogen chloride gas was passed into the solution until all the diazoketone had been consumed. The solution was washed with brine, dried over magnesium sulphate and evaporated. The title compound (2.44g) was isolated by column chromatography using gradient elution (silica gel, 4:1 going to 1:1 hexane : ethyl acetate); vmax (film) 1740cm-1 ; δH (CDCl3) 1.6-2.35 (4H,m), 3.30-3.75 (2H,m), 3.37 (3H,s) and 4.05-4.75 (4H,m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06020329
Source datasetuspto-grants-2000_02
ORD IDord-778eefff638942efae0b48d9bdb267c8
Source noteuspto-grants-2000_02