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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871100Generated: November 3, 2026

Tetramethyl orthocarbonate → 4-benzyloxy-2-methoxy-1-methyl-1H-benzimidazole

https://huagongshe.com/reaction/1871100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethyl orthocarbonateHCID 74613—
Reactant2-amino-3-benzyloxy-N-methylanilineHCID 10489541—
SolventAcetic AcidHCID 176—
Product4-benzyloxy-2-methoxy-1-methyl-1H-benzimidazoleHCID 10754361—

Reaction Steps

To a stirred solution of 2-amino-3-benzyloxy-N-methylaniline (318.5 mg) in acetic acid (3.2 ml) was added tetramethyl orthocarbonate (223.0 μl) at ambient temperature, and the reaction mixture was stirred for 4 hours. The reaction mixture was concentrated in vacuo, and to the residue were added ethyl acetate and a saturated sodium bicarbonate solution. The organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue was triturated with n-hexane-diisopropyl ether to give 4-benzyloxy-2-methoxy-1-methyl-1H-benzimidazole (273.3 mg) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06100284
Source datasetuspto-grants-2000_08
ORD IDord-d0ecd894acb74a538546d69f0a9fe56c
Source noteuspto-grants-2000_08