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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258149Generated: October 26, 2026

1-Pentanol → 1,2,3,3a,8,8a-Hexahydro-alpha-oxo-1,3a,8-trimethyl-5-pyrrolo[2,3-b]indole acetic acid, n-pentyl ester

https://huagongshe.com/reaction/258149

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PentanolHCID 6276—
Reactant1,2,3,3a,8,8a-Hexahydro-alpha-oxo-1,3a,8-trimethyl-5-pyrrolo[2,3-b]indole acetic acid, ethyl esterHCID 86746418—
CatalystTitanium tetraethoxideHCID 76524—
Product1,2,3,3a,8,8a-Hexahydro-alpha-oxo-1,3a,8-trimethyl-5-pyrrolo[2,3-b]indole acetic acid, n-pentyl esterHCID 86746424—

Reaction Steps

A solution of 1,2,3,3a,8,8a-hexahydro-α-oxo-1,3a,8-trimethyl-5-pyrrolo[2,3-b]indole acetic acid, ethyl ester (2.89 g) in 1-pentanol (61 ml) was treated at 0° C. under a nitrogen atmosphere with titanium (IV) ethoxide (0.80 ml). The solution was warmed to room temperature and then slowly heated for 2.5 hours keeping the temperature between 60°-80° C. The excess 1-pentanol was removed by distillation under high vacuum. The residue was washed successively with 50 ml of saturated aqueous NH4Cl solution, two 100 ml portions of saturated aqueous NaHCO3 solution and 50 ml of brine. The organic phase was dried (Na2SO4), filtered and concentrated to afford an oil which was purified by chromatography using preparative HPLC (silica gel, 5% methanol in ethyl acetate). The appropriate fractions were combined and concentrated under vacuum to yield 2.2 g of 1,2,3,3a,8,8a-hexahydro-α-oxo-1,3a,8-trimethyl-5-pyrrolo[2,3-b]indole acetic acid, n-pentyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05264587
Source datasetuspto-grants-1993_11
ORD IDord-4504591bdbd24325bcc6cc9b408ccc1c
Source noteuspto-grants-1993_11