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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406743Generated: October 30, 2026

Triethylamine → (2,4-Bis-benzyloxy-5-isopropyl-phenyl)-(5-nitro-1,3-dihydro-isoindol-2-yl)methanone

https://huagongshe.com/reaction/1406743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantTrifluoroacetateHCID 84468—
Reactant5-NitroisoindolineHCID 6424469—
Reactant2,4-Dibenzyloxy-5-isopropyl-benzoic acidHCID 59167879—
SolventDimethylformamideHCID 6228—
Product(2,4-Bis-benzyloxy-5-isopropyl-phenyl)-(5-nitro-1,3-dihydro-isoindol-2-yl)methanoneHCID 66672501—

Reaction Steps

A solution of 2,4-bis-benzyloxy-5-isopropyl-benzoic acid (505 mg; 1.3 mmol) (Preparation B5), 5-nitroisoindoline, trifluoroacetate (360 mg; 1 equiv.), EDAC (300 mg; 1.2 equiv.), HOBt (210 mg; 1.2 equiv.) and NEt3 (270 μl; 1.5 equiv.) in DMF (10 ml) was stirred at room temperature overnight then evaporated in vacuo. The residue was partitioned between EtOAc and 2M HCl, the EtOAc layer was separated, washed with saturated NaHCO3, dried (MgSO4) and evaporated. Purification by flash column chromatography (1:4 then 1:2 then 1:1 EtOAc/P.E. as eluant) gave 460 mg of (2,4-bis-benzyloxy-5-isopropyl-phenyl)-(5-nitro-1,3-dihydro-isoindol-2-yl)methanone. MS: [M+H]+ 523.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916552B2
Source datasetuspto-grants-2014_12
ORD IDord-3ac477413a9b43efaf4580ca68d9e6bf
Source noteuspto-grants-2014_12