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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424438Generated: October 30, 2026

Sodium hydride → HCID 66704009, compound

https://huagongshe.com/reaction/424438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantPyrrolidineHCID 31268—
ReactantHCID 66703997HCID 66703997—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66704009HCID 6670400958%

Reaction Conditions

Temperature80 °C

Reaction Steps

tert-Butyl (2S)-2-(4-(3-bromopropyloxy)phenyl)morpholine-4-carboxylate (2.0 g, 5.0 mmol) was added to a solution of sodium hydride (60% in oil, 0.22 g, 5.50 mmol) and pyrrolidine (0.43 g, 6.05 mmol) in tetrahydrofuran (40 ml) at room temperature and the mixture was stirred at 80° C. for 5 hours. The mixture was partitioned between water and chloroform. The organic layer was washed with brine, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting 5-10% methanol in chloroform to furnish tert-butyl (2S)-2-(4-(3-(pyrrolidin-1-yl)propyloxy)phenyl)morpholine-4-carboxylate (1.13 g, 58%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106045B2
Source datasetuspto-grants-2012_01
ORD IDord-b089b24c641449d19e251ab70f9b1ef6
Source noteuspto-grants-2012_01