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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040472Generated: October 31, 2026

Sodium hydride → HCID 11713695, compound

https://huagongshe.com/reaction/2040472

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 numberUS08580840B2
Source datasetuspto-grants-2013_11
ORD IDord-0dc2de93c9d24a9199a7a0e49f22dce8
Source noteuspto-grants-2013_11