HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661807Generated: November 1, 2026
1-Bromodecane → 5,10,15-tris-(4-Hydroxy-phenyl)-20-(4-decyloxy-phenyl)-porphyrin
https://huagongshe.com/reaction/661807
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromodecane | HCID 8173 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5,10,15,20-Tetrakis(4-hydroxyphenyl)porphyrin | HCID 135438030 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5,10,15-tris-(4-Hydroxy-phenyl)-20-(4-decyloxy-phenyl)-porphyrin | HCID 135916063 | — |
Reaction Steps
5,10,15,20-tetrakis-(4-Hydroxy-phenyl)-porphyrin (100 mg, 0.15 mmol) is dissolved and K2CO3 (230 mg) is suspended in DMF (30 mL). To the vigorously stirred reaction mixture a solution of 1-bromodecane (0.016 mL, 0.11 mmol) in DMF (10 mL) is added dropwise at 70° C. during 30 mins and the mixture is stirred for 1.5 h. After evaporation of solvent, the residue is dissolved in toluene:ethanol (1:1 by vol., ca. 3 mL) and purified by chromatography on a column (150 g) of silica gel (Merck 60) using toluene as eluent. After elution of the first 3 fractions, the column is eluted with toluene:ethyl acetate (2:1 by vol.) and the 5th fraction eluted is collected, the solvent removed and the residue dried under high vacuum to give the product as violet crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08084602B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-d78f0b03ab9c41e79d797c1537823fed |
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| Source note | uspto-grants-2011_12 |
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