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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22277851HCID 22277851—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductPhenol, 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967220B2
Source datasetuspto-grants-2005_11
ORD IDord-981a46114f4f42069dc61846e4588891
Source noteuspto-grants-2005_11