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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211975Generated: October 31, 2026

3,4-Dichlorobenzoic acid → tert-Butyl[(2S)-4-(3,4-dichlorobenzoyl)morpholin-2-yl]methylcarbamate

https://huagongshe.com/reaction/2211975

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzoic acidHCID 5817—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(R)-2-N-Boc-aminomethylmorpholineHCID 42556135—
SolventDimethylformamideHCID 6228—
Producttert-Butyl[(2S)-4-(3,4-dichlorobenzoyl)morpholin-2-yl]methylcarbamateHCID 8676023286%

Reaction Conditions

Temperature20 °C

Reaction Steps

A mixture of 3,4-dichlorobenzoic acid (0.5 g), 1-hydroxybenzotriazole (0.376 g), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.4329), and N,N-diisopropylethylamine (0.485 ml) in N,N-dimethylformamide (10 ml) was stirred at 20° C. for 10 min. The mixture was treated with tert-butyl (2R)-morpholin-2-ylmethylcarbamate (0.500 g, known compound WO 9639407A1) and stirred at 20° C. for 24 h. The mixture was partitioned between ethyl acetate (75 ml) and 2N aqueous hydrochloric acid (50 ml). The phases were separated and the organic extract washed with 2N aqueous hydrochloric acid (50 ml), saturated aqueous sodium hydrogen carbonate (2×50 ml), dried (MgSO4) and filtered. The solvent was removed in vacuo to give the title compound as a yellow oil, (0.774 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101882B2
Source datasetuspto-grants-2006_09
ORD IDord-24eec11b523c4c5899e1ee063f0c5a7a
Source noteuspto-grants-2006_09