HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437917Generated: November 1, 2026
Methoxyacetic Acid → HCID 21427270, compound
https://huagongshe.com/reaction/437917
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methoxyacetic Acid | HCID 12251 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 21427288 | HCID 21427288 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 21427270 | HCID 21427270 | — |
Reaction Steps
At maximally 10° C., 29.0 ml. of thionyl chloride is added dropwise under agitation to 28.2 ml. of methoxyacetic acid in 100 ml. of dimethylacetamide within 40 minutes. After, at 0° C., the reaction mixture has been agitated for another 2 hours, 63.0 g. (0.1 mole) of N-(3-carboxy-5-amino-2,4,6-triiodobenzoyl)-glycine methylamide (IVa), m.p. 252°-253° C. (decomposition), in 100 ml. of dimethylacetamide is added dropwise under agitation to the reaction mixture at maximally 8° C. during the course of one hour. Then, the solution is agitated overnight. After the addition of 5 ml. of water, the mixture is concentrated under vacuum, the residue is stirred with 700 ml. of water, the precipitate is vacuum-filtered, carefully washed with water, and, while still moist, reprecipitated from dilute ammonia with concentrated hydrochloric acid. After allowing the mixture to stand for some time, the acid is vacuum-filtered, washed well with water, stirred with fresh water, and, after another filtering step, dried under vacuum at 70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04032567 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-f25bec8cd4c04d0989e280811c3fd0b2 |
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| Source note | uspto-grants-1977_06 |
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