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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710234Generated: October 30, 2026

Water → tert-Butyl 2-(4-(1H-benzo[d]imidazol-2-yl)phenyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/710234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantO-PhenylenediamineHCID 7243—
ReactantSodium PyrosulfiteHCID 656671—
ReactantTert-butyl 2-(4-formylphenyl)morpholine-4-carboxylateHCID 87320997—
SolventDimethylacetamideHCID 31374—
Producttert-Butyl 2-(4-(1H-benzo[d]imidazol-2-yl)phenyl)morpholine-4-carboxylateHCID 13173392685.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

tert-Butyl 2-(4-formylphenyl)morpholine-4-carboxylate (300 mg, 1.03 mmol) was dissolved in dimethylacetamide (4.5 ml). 1,2-Diaminobenzene (134 mg, 1.24 mmol) and sodium metabisulfite (294 mg, 1.54 mmol) were added and the reaction mixture was stirred at 90° C. overnight. After cooling, the reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was dried over MgSO4 and evaporated. The crude material was purified by flash chromatography (20 g silica gel, 40 to 70% ethyl acetate in heptane) to yield a white solid (333 mg, 85%). MS (ISP): 280.3 (100%, [M-BOC+H]+), 380.2 (20%, [M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181230B2
Source datasetuspto-grants-2015_11
ORD IDord-3f9f9993d34543faab8c9271b21f29fd
Source noteuspto-grants-2015_11