HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277342Generated: October 27, 2026
Phthalic Anhydride → HCID 22628889, compound
https://huagongshe.com/reaction/277342
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | HCID 22628891 | HCID 22628891 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 22628889 | HCID 22628889 | — |
Reaction Steps
475.6 mg (0.50 mmol) of 8,20-bis-(4-aminobenzyl)-5,11,17,23-tetraisobutyl-2,4,10,14,16,22-hexamethyl-1,7,13,19-tetraoxa-4,10,16,22-tetraaza-cyclotetracosan-6,9,12,18,21,24-hexaone (for example from Example 4) were initially charged in 1.5 ml of glacial acetic acid and heated under reflux with 162.9 mg (1.1 mmol) of phthalic anhydride for 5 h. The mixture was concentrated, the residue was taken up in tertbutyl methyl ether (MTBE) and washed with sodium bicarbonate solution and saturated sodium chloride solution. The solution was dried with sodium sulfate, reconcentrated and subsequently filtered over a short silica gel column (Ø=3 cm, l=5 cm) using cyclohexane/ethyl acetate 2:1. Evaporation of the filtrate gave 0.55 g of slightly contaminated 8,20-bis-(4-phthalimidobenzyl)-5,11,17,23-tetraisobutyl-2,4,10,14,16,22-hexamethyl-1,7,13,19-tetraoxa-4,10,16,22-tetraaza-cyclotetracosan-6,9,12,18,21,24-hexaone as a yellow foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06355615B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-688001a3d25841e4aacae7e32f62516f |
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| Source note | uspto-grants-2002_03 |
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