HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609158Generated: October 31, 2026
Sodium Carbonate → 2,4,6-Trichloropyrimidine-5-carboxylic acid
https://huagongshe.com/reaction/1609158
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,4,6-Trichloropyrimidine-5-carbonyl chloride | HCID 13264361 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2,4,6-Trichloropyrimidine-5-carboxylic acid | HCID 20083957 | — |
Reaction Steps
A solution of 12.35 parts of trichloropyrimidine-5-carbonyl chloride in 200 parts by volume of acetone is stirred into a suspension of 12.12 parts of γ-(β-sulfatoethylsulfonyl)-propylamine in 250 parts by volume of acetone at 0° C. The reaction is carried out at 5° to 10° C., while maintaining a pH of 6.5 by means of 15% strength aqueous sodium carbonate solution. The trichloro-pyrimidine-5-carboxylic acid compound thus obtained of the formula ##STR25## is isolated by evaporation of the solution under reduced pressure. The compound is a solid substance; it is characterized by the following 13C-NMR spectroscopy values in hexadeutero-dimethyl sulfoxide: δ (in ppm)=21.7; 37.9; 51.2; 52.3; 60.0; 129.4; 157.5; 159.4; 160.6 compared with tetramethylsilane as the internal standard.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05399674 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-0d1725c573794696b56a8739192d6156 |
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| Source note | uspto-grants-1995_03 |
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