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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338967Generated: October 25, 2026

Tetrahydrofuran → (R)-7-(1-methoxypropan-2-yloxy)-2-methylquinoline

https://huagongshe.com/reaction/338967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(2S)-1-methoxypropan-2-olHCID 6993459—
Reactant2-Methylquinolin-7-olHCID 135451969—
SolventWaterHCID 962—
Product(R)-7-(1-methoxypropan-2-yloxy)-2-methylquinolineHCID 8670748473.2%

Reaction Steps

To a solution of 2-methylquinolin-7-ol (0.20 g, 1.3 mmol) in tetrahydrofuran (1.1 mL, 1.3 mmol) was added triphenylphosphine (0.82 g, 3.1 mmol), diethyl azodicarboxylate (0.32 mL, 2.0 mmol), and (S)-1-methoxypropan-2-ol (0.16 mL, 1.6 mmol) and the resultant mixture allowed to stir at ambient temperature for 24 hours. The reaction mixture was diluted with water (10 mL) and extracted with dichloromethane (2×20 mL). The combined organic extracts dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification by reverse phase chromatography on C18 (0-80% acetonitrile/water) afforded the title compound (0.22 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-2c8d10cbb8e1476399fa16159c03c6e6
Source noteuspto-grants-2014_11