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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874789Generated: October 26, 2026

Triphenylphosphine → methyl 5-{[(2,2-dimethyl-1,3-dioxan-5-yl)methyl]oxy}-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1874789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(2,2-Dimethyl-1,3-dioxan-5-yl)methanolHCID 3584869—
Reactantmethyl 5-hydroxy-1H-indole-2-carboxylateHCID 21904362—
SolventDichloromethaneHCID 6344—
Productmethyl 5-{[(2,2-dimethyl-1,3-dioxan-5-yl)methyl]oxy}-1H-indole-2-carboxylateHCID 5945136093.9%

Reaction Steps

Methyl 5-Hydroxy-1H-indole-2-carboxylate (0.10 g, 0.5 mmol), triphenylphosphine (0.28 g, 1.0 mmol), diethyl azodicarboxylate (0.18 g, 1.0 mmol) and (2,2-dimethyl-1,3-dioxan-5-yl)methanol (0.15 g, 1.0 mmol) were dissolved in CH2Cl2 (5 mL) and the mixture was stirred overnight. The solvent was evaporated. Purification was accomplished by Reverse-Phase HPLC (water/acetonitrile with 0.1% TFA). The desired fractions were neutralized with saturated NaHCO3 and extracted with EtOAc. The organic extracts were combined dried over Na2SO4, filtered and evaporated to afford the title compound (0.15 g, 90%) as a tan solid. 1H NMR (400 MHz, DMSO-d6): δ ppm 11.74 (br. s., 1H), 7.29 (d, 1H), 7.09 (d, 1H), 7.01 (d, 1H), 6.88 (dd, 1H), 3.92-4.01 (m, 4H), 3.81 (s, 3H), 3.72 (dd, 2H), 1.97-2.08 (m, 1H), 1.31 (s, 3H), 1.28 (s, 3H). MS: m/z 342.2 (M+23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-bdf74f0af1ba40a5a3fb1d0cdcebe4b8
Source noteuspto-grants-2012_11