HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109657Generated: October 25, 2026
Succinyl chloride → Succinic acid bis(3,4-dibenzyloxybenzylamide)
https://huagongshe.com/reaction/2109657
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Succinyl chloride | HCID 10970 | — |
| Reactant | 3,4-Dibenzyloxybenzylamine | HCID 21821660 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Succinic acid bis(3,4-dibenzyloxybenzylamide) | HCID 57634450 | — |
Reaction Steps
3,4-dibenzyloxybenzylamine (1.1 g, 3.45 mmol) was dissolved in anhydrous pyridine (8 ml) and cooled to 0° C. with stirring under nitrogen. To this solution, succinyl chloride (0.23 g, 1.42 mmol) was added dropwise over 30 minutes as a solution in dichloromethane (50 ml), while maintaining the reaction mixture at 0° C. The reaction was allowed to warm to room temperature and stirred for an additional 45 minutes. The reaction was poured onto crushed ice (70 g) and the dichloromethane layer was separated. The organic extract was washed with dilute aqueous hydrochloric acid (2×20 ml of 0.1M solution), water (20 ml), and dried (Na2SO4). Removal of the solvent at reduced pressure afforded a crude solid, which was triturated with methanol (5 ml) to afford after filtration the protected diamide, yield 300 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514583B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-9b689f76e162474ba3ecd3f488feca22 |
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| Source note | uspto-grants-2009_04 |
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