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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588016Generated: October 25, 2026

Hydrochloric Acid → (S)-3-[1-(2,3,6-Trichlorophenoxy)prop-2-ynyl]pyrrolidine

https://huagongshe.com/reaction/588016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantPhenolHCID 996—
ReactantTolueneHCID 1140—
ReactantTriphenylphosphineHCID 11776—
Reactant2,3,6-TrichlorophenolHCID 13618—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant(S)-3-(1-Hydroxyprop-2-ynyl)pyrrolidine-1-carboxylic Acid t-Butyl EsterHCID 58104606—
Product(S)-3-[1-(2,3,6-Trichlorophenoxy)prop-2-ynyl]pyrrolidineHCID 58104602—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (S)-3-(1-hydroxyprop-2-ynyl)pyrrolidine-1-carboxylic acid t-butyl ester (21.0 mg, 93.2 μmol) and DIAD (22.0 μL, 112 μmol) was dissolved in toluene (65 μL, 610 μmol) at room temperature. PPh3 (29.3 mg, 112 μmol) and 2,3,6-trichlorophenol (20.2 mg, 102 μmol) were dissolved in toluene (0.1 mL, 1 mmol) and heated at 100° C. The t-butyl ester mixture was slowly added into the phenol mixture at 100° C., and stirred for 1 hour. The mixture was then removed from the heat and stirred at room temperature overnight. The mixture was then concentrated and the resulting residue was treated with 1.25M HCl in EtOH (0.6 mL, 0.8 mmol) at room temperature overnight. The mixture was concentrated and the residue was redissolved in a mixture of 50% AcOH/H2O (1.4 mL) and McCN (0.2 mL), filtered and purified by reverse phase preparative HPLC to yield the title compound as a mono-TFA salt (21.2 mg, 99% purity). MS in/z: [M+H]+ calcd for C13H12Cl3NO, 304.00. found 304.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227933B2
Source datasetuspto-grants-2016_01
ORD IDord-bd778949c447438a8b71187d81362d7f
Source noteuspto-grants-2016_01