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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715965Generated: October 30, 2026

Sodium triacetoxyborohydride → methyl 7-nitro-2,3,9,9a-tetrahydro-1H-pyrrolo[1,2-a]indole-8-carboxylate

https://huagongshe.com/reaction/715965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactantmethyl 7-nitro-2,3-dihydro-1H-pyrrolo[1,2-a]indole-8-carboxylateHCID 70984130—
SolventTolueneHCID 1140—
SolventTrifluoroacetic acidHCID 6422—
Productmethyl 7-nitro-2,3,9,9a-tetrahydro-1H-pyrrolo[1,2-a]indole-8-carboxylateHCID 70983689164.7%

Reaction Steps

Methyl 7-nitro-2,3-dihydro-1H-pyrrolo[1,2-a]indole-8-carboxylate (Intermediate 19, 1.00 g) was dissolved in TFA (100 ml) and sodium triacetoxyborohydride (8.11 g) was added. The reaction mixture was stirred at room temperature, then diluted with toluene and concentrated in vacuo. The residue was dissolved in aqueous potassium carbonate solution and extracted with ethyl acetate, dried (MgSO4) and filtered. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM, with a gradient of 0-2% to give methyl 7-nitro-2,3,9,9a-tetrahydro-1H-pyrrolo[1,2-a]indole-8-carboxylate (1.66 g) as a yellow gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187494B2
Source datasetuspto-grants-2015_11
ORD IDord-7bd2c8e6444f4da3a65a1dc3fa5c5150
Source noteuspto-grants-2015_11