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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393470Generated: October 30, 2026

Methyl 4-(indol-3-yl)butyrate → 4-(1H-indol-3-yl)butan-1-ol

https://huagongshe.com/reaction/2393470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(indol-3-yl)butyrateHCID 85010—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product4-(1H-indol-3-yl)butan-1-olHCID 11171478107%

Reaction Steps

A tetrahydroturan solution (500 ml) of methyl 4-(3-indolyl)-butyrate (103 g) was added dropwise to a suspension of lithium aluminium hydride (25 g) in tetrahydrofuran (1000 ml) at 40° C. followed by stirring for 1 h at room temperature. Usual work-up gave 4-(3-indolyl)-1-butanol (96 g) as an oil. Arylation with 1-fluoro-4-iodobenzene according to the method described in EXAMPLE 5 yielded 4-[1-[4-fluorophenyl)-3-indolyl]-1-butanol which was converted to the title compound 9a by the method described in EXAMPLE 2 using spiro[1H-2-benzopyran-4(3H),4'-piperidine]. The maleate salt crystallized from acetone by addition of maleic acid. Yield: 1.5 g, mp: 189°-90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05807871
Source datasetuspto-grants-1998_09
ORD IDord-118ac1b19e8e4e869ffb822c6cc31296
Source noteuspto-grants-1998_09