HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271813Generated: October 30, 2026
Diethyl Ether → 2,4,6-Triiodo-1,3,5-tris-(aminoethoxymethyl)benzene
https://huagongshe.com/reaction/1271813
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,4,6-Triiodo-1,3,5-tris-(2-tert-butoxycarbonylaminoethoxymethyl)benzene | HCID 18454888 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,4,6-Triiodo-1,3,5-tris-(aminoethoxymethyl)benzene | HCID 86595649 | — |
Reaction Steps
24.4 g (25 mmol) of 2,4,6-triiodo-1,3,5-tris-(2-tert-butoxycarbonylaminoethoxymethyl)benzene is dissolved in 100 ml of dichloromethane, mixed at 0° C. with 100 ml of trifluoroacetic acid and stirred for 3 hours at 0° C. The batch is poured into 500 ml of diethyl ether, the solid that accumulates in this case is suctioned off and rewashed several times with diethyl ether. The residue is dissolved in 100 ml of water and 100 ml of dichloromethane while being stirred vigorously, and 32% NaOH solution is added until a pH of 10 is reached. The organic phase is separated, the aqueous phase is extracted three times with 50 ml each of dichloromethane, the combined organic phases are dried on magnesium sulfate and evaporated to the dry state.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07208140B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-2a0584e5107a4ab896d189fb059aa205 |
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| Source note | uspto-grants-2007_04 |
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