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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642774Generated: October 30, 2026

Sodium hydride → HCID 11713695, compound

https://huagongshe.com/reaction/642774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 11515692HCID 11515692—
Reactant2-[4-(Chloromethyl)phenoxy]-N,N-diethylethan-1-amine--hydrogen chloride (1/1)HCID 12493692—
SolventDimethylformamideHCID 6228—
ProductHCID 11713695HCID 11713695—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 7-benzyloxy-3-methoxy-10H-benzo[4,5]furo[3,2-b]indole (102 mg, 0.297 mmol) in DMF (5 mL) was added NaH (37 mg, 60% in mineral oil, 3.0 eq.) followed by [2-(4-chloromethyl-phenoxy)-ethyl]-diethyl-amine hydrochloride salt (99 mg, 0.356 mmol) at 0° C. The mixture was stirred at 0° C. for 30 minutes, warmed to 25° C., and quenched by NH4Cl (solid). EtOAc and water were then added to the mixture. The reaction mixture was then partitioned between EtOAc and water. The aqueous layer was extracted three times with EtOAc. The combined organic layer was washed with brine, dried over anhydrous Na2SO4, filtered and concentrated to yield crude material. The crude material was purified by silica gel (EtOAc to CH2Cl2: MeOH 5:1) to yield the title compound as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696239B2
Source datasetuspto-grants-2010_04
ORD IDord-09a6ff24f2934a82a91dcded425089cf
Source noteuspto-grants-2010_04