HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728539Generated: October 29, 2026
N-Hydroxysuccinimide → HCID 86746027, compound
https://huagongshe.com/reaction/1728539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 19014054 | HCID 19014054 | — |
| Reactant | 2-(Methyldisulfanyl)ethan-1-amine | HCID 21832734 | — |
| Reactant | 131027-12-8 | HCID 85609996 | — |
| Reactant | HCID 86746028 | HCID 86746028 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86746027 | HCID 86746027 | — |
Reaction Steps
To a solution of m-(carboxymethoxy)phenyl acetone (6.1 g, 0.029 mmole) in N,N-dimethylformamide (56 ml, dried over molecular sieves, 3A) were added under nitrogen at 5° powdered 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDCI, 6.1 g, 0.032 mole) and N-hydroxysuccinimide (3.7 g, 0.032 mole). The resulting reaction mixture was then allowed to stir at 5° overnight. The complete formation of N-hydroxysuccinimic ester was observed. To the methyldithioethylamide hydrochloride (4.7 g, 0.029 mole, prepared in D above) in water (20-50 ml) was added triethylamine to adjust the pH to 8.5. Then the N-hydroxysuccinimic ester of m-(carboxymethoxy)phenyl acetone was added dropwise to the methyldithioethylamine solution with the adjustment of pH to 8.5, and the resulting solution was allowed to stir at 5° for 1 hour. Additional reagents, methyldithioethylamine hydrochloride (2 g, 0.0125 mole) and EDCI (3.0 g, 0.0156 mole), were added and the pH of the resulting solution was adjusted to 6.5 and the reaction mixture was allowed to stir at 5° overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05328828 |
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| Source dataset | uspto-grants-1994_07 |
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| ORD ID | ord-122368b0ecb54adaad12abe425fc152b |
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| Source note | uspto-grants-1994_07 |
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