Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101518Generated: October 31, 2026

3-Aminophenol → 3-[1-(3,5-Dichloro-benzyl)-1H-imidazol-2-ylmethoxy]-phenylamine

https://huagongshe.com/reaction/2101518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminophenolHCID 11568—
ReactantSodium hydrideHCID 24758—
Reactantchloromethyl-1-(3,5-dichlorobenzyl)-1H-imidazole hydrochlorideHCID 68862721—
SolventDimethylformamideHCID 6228—
Product3-[1-(3,5-Dichloro-benzyl)-1H-imidazol-2-ylmethoxy]-phenylamineHCID 1195107070%

Reaction Steps

3-Aminophenol (87 mg, 0.8 mmol) was dissolved in DMF and NaH (33 mg, 0.83 mmol) was added. After 10 min, 2-(chloromethyl)-1-(3,5-dichlorobenzyl)-1H-imidazole hydrochloride (see Example 1) (100 mg, 0.32 mmol) was added in one portion. After 20 min, the reaction was partitioned between water (10 mL) and EtOAc (10 mL). The layers were separated and the aqueous layer was re-extracted with EtOAc (1×10 mL). The combined organic layers were washed with 1M NaOH (3×10 mL), water (10 mL) and brine, dried over MgSO4, filtered and concentrated to yield the title compound as a pale yellow oil (78 mg, 70%); MS m/z 348 [C17H15Cl2N3O+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572921B2
Source datasetuspto-grants-2009_08
ORD IDord-677a91aa325b4fada7c1c34c13ba73ce
Source noteuspto-grants-2009_08