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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906521Generated: October 30, 2026

p-Toluenesulfonic acid monohydrate → 2-Amino-5-(1-isopropoxy-propyl)-4-trifluoromethyl-benzoic acid methyl ester

https://huagongshe.com/reaction/906521

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2-Acetylamino-5-(1-hydroxy-propyl)-4-trifluoromethyl-benzoic acid methyl esterHCID 59164458—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
Product2-Amino-5-(1-isopropoxy-propyl)-4-trifluoromethyl-benzoic acid methyl esterHCID 1196538238.5%

Reaction Steps

A solution of 2-acetylamino-5-(1-hydroxy-propyl)-4-trifluoromethyl-benzoic acid methyl ester (394 mg, 1.23 mmol) in 2-propanol (2 mL) at room temperature was treated with p-toluenesulfonic acid monohydrate (75.3 mg, 0.39 mmol) and the reaction was stirred for 13 d at r.t. The reaction mixture was diluted with water and EtOAc and basified to pH 8 with sat. aq KHCO3. The organic phase was washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by flash chromatography (20 g of silica gel, EtOAc/hexanes (0:1→3:7)) to give the title product (48 mg, 12%). as colorless crystals. m.p.: 54-56° C., ESI-MS: m/z 320 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012988B2
Source datasetuspto-grants-2011_09
ORD IDord-2a801ede61344c3c91cbc53870fcc1ab
Source noteuspto-grants-2011_09