HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902605Generated: October 29, 2026
Dimethylformamide → 5-Methoxyacetylamino-2,4,6-triiodoisophthalic acid (2,3-dihydroxypropyl)amide chloride
https://huagongshe.com/reaction/1902605
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | 3-Amino-1,2-propanediol | HCID 73561 | — |
| Reactant | 5-Methoxyacetamido-2,4,6-triiodoisophthaloyl chloride | HCID 13589961 | — |
| Product | 5-Methoxyacetylamino-2,4,6-triiodoisophthalic acid (2,3-dihydroxypropyl)amide chloride | HCID 86650908 | — |
Reaction Steps
50 g. (75 mmol) of 5-methoxyacetylamino-2,4,6-triiodoisophthalic acid dichloride is dissolved in 200 ml. of dry DMF; 18 g. (97.3 mmol) of tributylamine is added thereto, the mixture is heated to 60° C., and, at this temperature, a solution of 7.5 g. (82.4 mmol) of 2,3-dihydroxypropylamine in 50 ml. of DMF is added dropwise thereto. The mixture is stirred for 2 hours at 60° C., then concentrated to 100 ml., and stirred into 1.2 l. of methylene chloride. The precipitate thus formed is vacuum-filtered, dried, refluxed twice with respectively 500 ml. of ethyl acetate, and filtered in the hot state. The evaporated filtrate yields 40.5 g. (56 mmol)=74.5% of theory of the desired product as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04364921 |
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| Source dataset | uspto-grants-1982_12 |
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| ORD ID | ord-875430f714694d3185cad83fec7dfa28 |
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| Source note | uspto-grants-1982_12 |
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