HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063871Generated: November 1, 2026
HCID 22277851, compound → Phenol, 4-[4-[(hydroxyamino)methyl]-2,6-diiodophenoxy]-
https://huagongshe.com/reaction/1063871
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22277851 | HCID 22277851 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Phenol, 4-[4-[(hydroxyamino)methyl]-2,6-diiodophenoxy]- | HCID 22277849 | — |
Reaction Steps
A solution containing tert-butyl N-(tert-butoxycarbonyloxy)-N-[3,5-diiodo-4-(4-hydroxyphenoxy)benzyl]carbamate (150 mg, 0.21 mmol) in 4 ml of 30% TFA in CH2Cl2 was stirred for 2 h and then evaporated to dryness to afford 4-(4-hydroxyaminomethyl-2,6-diiodophenoxy)phenol (M+1=484). This residue was then treated with triethylamine (0.5 ml) and the mixed anhydride (0.5 ml) [made from formic acid and acetic anhydride (1:2 v/v) at 50° C. for 1 h] in 2 ml of CH2Cl2 for 0.5 h. All volatiles were removed and the residue dissolved in methanol then treated with 10% NaOH for 0.5 h. This was diluted with ethyl acetate and water and adjusted to pH of 6. The layers were separated and the organic extract was evaporated in vacuo. Purification by preparative HPLC afforded the title compound (27 mg, 25%) as an off white solid. 1H NMR (400 MHz, CD3OD): δ 8.38, 8.18* (s, 1H); 7.89*, 7.86 (s, 2H); 6.69 (d, j=8.8 Hz, 2H); 6.55 (d, j=8.8 Hz, 2H),; 4.67, 4.63* (s, 2H). M+1=512. *: minor rotamer
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06967220B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-981a46114f4f42069dc61846e4588891 |
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| Source note | uspto-grants-2005_11 |
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