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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399483Generated: October 27, 2026

1-Bromopentane → 1-Pentyl-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/1399483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopentaneHCID 8057—
ReactantSodium hydrideHCID 24758—
ReactantIndole-3-Carboxylic AcidHCID 69867—
SolventDimethylformamideHCID 6228—
Product1-Pentyl-1H-indole-3-carboxylic acidHCID 1738172349%

Reaction Steps

Indole 3-carboxylic acid (3 g, 18.62 mmol) was added to a suspension of sodium hydride (60% in oil) (1.11 g, 1.5 eq) in dry DMF (30 ml) under a nitrogen atmosphere. The mixture was stirred at room temperature for 45 min (H2 evolving has ceased) and to this was added 1-bromopentane (4.62 ml, 2 eq) in dry DMF (10 ml) dropwise. The mixture was stirred at room temperature overnight. The solvents were removed in vacuo and to the residue was added water (30 ml) and ethyl acetate (30 ml). The ethyl acetate portion was separated, dried over sodium sulphate, filtered and evaporated to dryness. The crude residue was purified by column chromatography (silica gel: 20% ethyl acetate in hexane) to give the title compound (2.12 g, 49%) as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906633B2
Source datasetuspto-grants-2014_12
ORD IDord-7034d79099a545cba19a65301d521710
Source noteuspto-grants-2014_12