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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73934Generated: October 26, 2026

2-Bromobutane → 3-sec-Butyl-1H-indol-6-ylamine

https://huagongshe.com/reaction/73934

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromobutaneHCID 6554—
Reactant6-Nitro-1H-indoleHCID 78502—
SolventAcetonitrileHCID 6342—
Product3-sec-Butyl-1H-indol-6-ylamineHCID 57470200—

Reaction Steps

3-sec-Butyl-1H-indol-6-ylamine (B-14) was synthesized following the general scheme above starting from 6-nitroindole and 2-bromobutane. Overall yield (20%). HPLC ret. time 2.32 min, 10-99% CH3CN, 5 min run; ESI-MS 189.5 m/z (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829204B2
Source datasetuspto-grants-2014_09
ORD IDord-9e49ae8cd83446ca958e78fb7ba17cdc
Source noteuspto-grants-2014_09