HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37302Generated: October 26, 2026
Triethylamine → HCID 178520458, compound
https://huagongshe.com/reaction/37302
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 3-Cyclododecylpropanoic acid | HCID 2729113 | — |
| Reactant | Thiotetronic acid | HCID 10214383 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 178520458 | HCID 178520458 | — |
Reaction Steps
To a solution of 0.80 g of thiotetronic acid in 20 ml of dry dimethylformamide at 0° C. is added 1.1 ml (836 mg, 8.3 mmol) of triethylamine and 0.31 g (2.5 mmol) of dimethylaminopyridine. After stirring for 5 minutes, 2.0 g (8.3 mmol) of 3-cyclododecylpropanoic acid is added followed by 1.6 g (8.3 mmol) of 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride. After 10 minutes the ice bath is removed and the reaction mixture is allowed to stir overnight at room temperature. The reaction mixture is then poured into 1N hydrochloric acid and extracted 3 times with ethyl acetate. The organic layers are combined, washed with brine, filtered and evaporated to give a brown oil. The oil is subjected to flash chromatography using acidic silica gel and hexane/ethyl acetate (9:1) as the mobile phase to give an off white solid: m.p. 60°-62° C.; IR (KBr) 2940, 1700, 1630, and 1590 cm1 : NMR (CDCl3) δ 1.33 (bs, 22H), 1.49 (bs, 1H), 1.58 (m, 2H), 2.96 (m, 2H), 3.77 and 3.98 (singlets, 2H); MS (EI) M+338.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420153 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-8ac26025b81d4095869c156cdcd07859 |
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| Source note | uspto-grants-1995_05 |
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