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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41103Generated: October 26, 2026

Acetic Acid → (R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/41103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Fluoro-3-nitrotolueneHCID 136287—
Reactant(R)-2-Aminomethyl-4-Boc-morpholineHCID 1515269—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
Product(R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylateHCID 6717027899.6%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of (R)-tert-butyl 2-(aminomethyl)morpholine-4-carboxylate (0.715 g, 3.31 mmol), DIPEA (0.577 mL, 3.31 mmol), and 1-fluoro-4-methyl-2-nitrobenzene (0.513 g, 3.31 mmol) in MeOH (14 mL) was heated at 140° C. in A microwave reactor for 30 min and then cooled to room temperature. Acetic acid (1.9 mL, 33.1 mmol) was added, followed by zinc (2.162 g, 33.1 mmol). The resulting mixture was stirred at room temperature for 90 min to afford the (R)-tert-butyl 2-((2-amino-4-methylphenylamino)methyl)morpholine-4-carboxylate product (1.06 g), which was used without further purification in the next step. The product was analyzed on analytical HPLC MS using the high pH gradient method (mobile phase: 5-95% B; A: H2O with 10 mM NH4CO3 and 0.375% NH4OH v/v; B: CH3CN; 2.25 min run; X-Bridge C18; column size: 2.1×30 mm; and particle size: 5 μm). MS m/z 322.4 [M+H]+ (ESI), Rt 1.80 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530467B2
Source datasetuspto-grants-2013_09
ORD IDord-48826e0ef53c44c2b9ad5f3907d5d719
Source noteuspto-grants-2013_09