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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301813Generated: October 30, 2026

Sodium borohydride → tert-Butyl 6-amino-1H-indole-1-carboxylate

https://huagongshe.com/reaction/2301813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl 6-nitro-1H-indole-1-carboxylateHCID 22240526—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 6-amino-1H-indole-1-carboxylateHCID 22240525—

Reaction Steps

To a stirring solution of 1-Boc-6-nitroindole (250 mg, 0.95 mmol) in THF (5 mL) and MeOH (10 mL) at 0° C., was added Ni(OAc)2.4H2O (473 mg, 1.9 mmol). After complete dissolution, NaBH4 (143 mg, 3.8 mmol) was added slowly. Upon addition of the NaBH4, the reaction mixture turned black and vigorous gas evolution was observed. After 15 min, the solvents were removed in vacuo and the residue was dissolved in a stirring mixture of ethyl acetate (100 mL), conc NH4OH (10 mL) and water (20 mL). The layers were separated and the organic phase was washed again with 33% conc NH40OH in water and then washed twice with brine. The organic phase was then dried with MgSO4, filtered and concentrated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500851B2
Source datasetuspto-grants-2002_12
ORD IDord-bf1aac73031447afbf5b1c48a23d26b5
Source noteuspto-grants-2002_12