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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404852Generated: October 31, 2026

Acetic Anhydride → HCID 59410103, compound

https://huagongshe.com/reaction/2404852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 22279241HCID 22279241—
SolventDichloromethaneHCID 6344—
ProductHCID 59410103HCID 5941010393%

Reaction Steps

To a solution of 4-cyclohexyl-3-nitro-aniline (1.54 g, 6.99 mmol) in DCM (15 mL) was added Et3N (1.9 mL, 13.63 mmol), followed by the addition of acetic anhydride (3.3 mL, 34.98 mmol). The reaction mixture was stirred at room temperature for 2 h, quenched with water, the layers separated and the organic layer was washed with 0.1N HCl, followed by washing with H2O. The organic layer was dried over MgSO4, filtered and concentrated to obtain N-(4-cyclohexyl-3-nitrophenyl)acetamide (1.7 g, 93%). 1H NMR (400 MHz, CDCl3) δ 7.91 (d, J=2.2 Hz, 1H), 7.69 (dd, J=8.6, 2.2 Hz, 1H), 7.52 (s, 1H), 7.40 (d, J=8.6 Hz, 1H), 3.01-2.87 (m, 1H), 2.22 (s, 3H), 1.95-1.78 (m, 5H), 1.42 (t, J=10.4 Hz, 4H), 1.32-1.21 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802700B2
Source datasetuspto-grants-2014_08
ORD IDord-45a4d2bff2f84bc9ae197e7285118580
Source noteuspto-grants-2014_08