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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587892Generated: October 25, 2026

Sodium borohydride → ethyl 6-(aminomethyl)-1-benzyl-5-fluoro-2,3-dihydro-1H-inden-2-ylcarbamate

https://huagongshe.com/reaction/587892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactantethyl 1-benzyl-6-cyano-5-fluoro-2,3-dihydro-1H-inden-2-ylcarbamateHCID 66741062—
ReactantHCID 178418361HCID 178418361—
CatalystDichlorocobalt hexahydrateHCID 517166—
SolventMethanolHCID 887—
Productethyl 6-(aminomethyl)-1-benzyl-5-fluoro-2,3-dihydro-1H-inden-2-ylcarbamateHCID 66740863—

Reaction Steps

To a solution of ethyl 1-benzyl-6-cyano-5-fluoro-2,3-dihydro-1H-inden-2-ylcarbamate (182 mg, 0.538 mmol) in methanol (5 ml) containing cobalt(II) chloride hexahydrate (256 mg, 1.076 mmol) was added sodium borohydride (203 mg, 5.38 mmol) in small portions with caution to control the evolution of hydrogen and the exothermic reaction (approximately 1 h). The reaction mixture was stirred at room temperature for 10 min and carefully quenched by addition of 12N hydrochloric acid until the black precipitate was dissolved. The reaction mixture was carefully made alkaline with concentrated ammonia and extracted with ethyl acetate, dried, filtered and evaporated to leave the crude product ethyl 6-(aminomethyl)-1-benzyl-5-fluoro-2,3-dihydro-1H-inden-2-ylcarbamate a pale brown oil. m=184 mg (quant.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227930B2
Source datasetuspto-grants-2016_01
ORD IDord-e3da100a67bc48c78f1f204d7da75df4
Source noteuspto-grants-2016_01