HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612296Generated: October 30, 2026
Oxalyl chloride → HCID 18780160, compound
https://huagongshe.com/reaction/612296
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 5-(Methoxymethyl)oxolane-2-carboxylic acid | HCID 18780016 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18780160 | HCID 18780160 | — |
Reaction Steps
A solution of (2RS,5SR)-5-methoxymethyltetrahydrofuran-2-carboxylic acid (3.1 g) in dichloromethane (50 ml) was treated with oxalyl chloride (2.68 ml) and dimethylformamide (1 drop). The mixture was stirred for 1 h 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 (100 ml) 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 0.5 h 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 (2.44 g) was isolated by column chromatography using gradient elution (silica gel, 4:1 going to 1:1 hexane : ethyl acetate); νmax (film) 1740 cm-1 ; δlH (CDCl3) 1.6-2.35 (4 H,m), 3.30-3.75 (2 H,m), 3.37 (3 H,s) and 4.05-4.75 (4 H,m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06001997 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-1a960a21190b48a9a170e20fdb2c80f9 |
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| Source note | uspto-grants-1999_12 |
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