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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443069Generated: October 31, 2026

Triphenylphosphine → HCID 86601371, compound

https://huagongshe.com/reaction/1443069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-EthoxyphenolHCID 66755—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Reactanttert-Butyl (2S)-2-(hydroxymethyl)morpholine-4-carboxylateHCID 1512577—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 86601371HCID 86601371—

Reaction Steps

To a stirring mixture at room temperature of (S)-2-hydroxymethyl-morpholine-4-carboxylic acid, tert-butyl ester, 2-ethoxyphenol and triphenylphosphine in DME was added dropwise diisopropyl azodicarboxylate. The solution was stirred at room temperature for 24 h, concentrated (to remove most of the DME), then suspended into hexanes. The solid that formed was filtered. The filtrate was concentrated, redissolved into diethyl ether, then washed with 1 N NaOH (2×), sat. KH2PO4 and brine solutions. The organic extract was dried (MgSO4), filtered, concentrated and chromatographed (MPLC, silica gel, 20% EtOAc in hexanes) to give (S)-2-(2-ethoxy-phenoxymethyl)-morpholine-4-carboxylic acid, tert-butyl ester as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659394B2
Source datasetuspto-grants-2010_02
ORD IDord-254ef95956994d71b89fb908439a1f75
Source noteuspto-grants-2010_02