HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908676Generated: October 27, 2026
Triethylamine → 2.2'-[(methylimino)dibutane-4,1-diyl]bis(1H-isoindole-1.3(2H)-dione)
https://huagongshe.com/reaction/908676
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(4-Bromobutyl)phthalimide | HCID 93575 | — |
| Reactant | 2-[4-(Methylamino)butyl]isoindoline-1,3-dione | HCID 59838176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2.2'-[(methylimino)dibutane-4,1-diyl]bis(1H-isoindole-1.3(2H)-dione) | HCID 67392620 | — |
Reaction Steps
209 mg (0.9 mmol) of 2-[4-(methylamino)butyl]-1H-isoindole-1.3(2H)-dione is solubilized in 5 ml of tetrahydrofuran, then 385 μl (2.7 mmol; 3 equivalents) of triethylamine and 254 mg (0.9 mmol; 1 equivalent) of 2-(4-bromobutyl)-1H-isoindole-1.3(2H)-dione are added to the reaction mixture which is maintained for 25 minutes under microwaves at 165° C. The precipitate obtained is filtered and the filtrate concentrated under reduced pressure. The expected product is purified by chromatography on a silica column (eluent: dichloromethane/methanol: 95/5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017637B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-0b6e342cbe124722bfcbc667e20f65ef |
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| Source note | uspto-grants-2011_09 |
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