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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671394Generated: October 26, 2026

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

https://huagongshe.com/reaction/1671394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantPhenolHCID 996—
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—
SolventTolueneHCID 1140—
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 μmmol) and DIAD (22.0 μL, 112 μmmol) was dissolved in toluene (65 μL, 610 μmmol) at room temperature. PPh3 (29.3 mg, 112 μmmol) and 2,3,6-trichlorophenol (20.2 mg, 102 μmmol) 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 MeCN (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 m/z: [M+H]+ calcd for C13H12Cl3NO, 304.00; found 304.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994209B2
Source datasetuspto-grants-2011_08
ORD IDord-8d4c5d4177814026bd8e1e6398f39400
Source noteuspto-grants-2011_08