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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728539Generated: October 29, 2026

N-Hydroxysuccinimide → HCID 86746027, compound

https://huagongshe.com/reaction/1728539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxysuccinimideHCID 80170—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 19014054HCID 19014054—
Reactant2-(Methyldisulfanyl)ethan-1-amineHCID 21832734—
Reactant131027-12-8HCID 85609996—
ReactantHCID 86746028HCID 86746028—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 86746027HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05328828
Source datasetuspto-grants-1994_07
ORD IDord-122368b0ecb54adaad12abe425fc152b
Source noteuspto-grants-1994_07