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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894036Generated: October 30, 2026

2-Amino-5-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-4-trifluoromethyl-benzoic acid methyl ester → 2-Amino-5-[3-(tetrahydro-pyran-2-yloxy)-propyl]-4-trifluoromethyl-benzoic acid methyl ester

https://huagongshe.com/reaction/1894036

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-4-trifluoromethyl-benzoic acid methyl esterHCID 59164421—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-5-[3-(tetrahydro-pyran-2-yloxy)-propyl]-4-trifluoromethyl-benzoic acid methyl esterHCID 5916451589.4%

Reaction Steps

A suspension of 2-amino-5-[3-(tetrahydro-pyran-2-yloxy)-prop-1-ynyl]-4-trifluoromethyl-benzoic acid methyl ester (2.20 g, 6.16 mmol) and palladium on carbon (250 mg, 10%) in THF (15 mL) was stirred at r.t. for 30 min under hydrogen (5 bars). The mixture was then filtered and concentrated in vacuo. The crude product was purified by flash chromatography (silica gel 60, hexanes/EtOAc 5:1) to afford 2-amino-5-[3-(tetrahydro-pyran-2-yloxy)-propyl]-4-trifluoromethyl-benzoic acid methyl ester (1.99 g, 5.51 mmol, 89%) as a colorless oil, ESI-MS: m/z 384 [M+Na]+, rt 6.20 min)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513268B2
Source datasetuspto-grants-2013_08
ORD IDord-075cd7b99e8f4c6497e2576cb54b5e4b
Source noteuspto-grants-2013_08