Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 14219918 | HCID 14219918 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22168546 | HCID 22168546 | — |
Reaction Steps
A 3.04 g portion of methyl 4-carboxymethylphenylacetate, prepared above, was dissolved in 50 mL of anhydrous tetrahydrofuran. After the addition of2.5 mL oxalyl chloride, the mixture was stirred for 4 hours. The solvents were evaporated under a stream of dry nitrogen as the flask was warmed to 45° C. Any remaining solvent or oxalyl chloride was then removed under high vacuum; the product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04868132 |
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| Source dataset | uspto-grants-1989_09 |
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| ORD ID | ord-8a8e2af98bb542d2b303768ccd815052 |
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| Source note | uspto-grants-1989_09 |
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