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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541798Generated: November 1, 2026

Triethylamine → HCID 57961752, compound

https://huagongshe.com/reaction/541798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzoyl chloride, 3-nitro-HCID 8495—
ReactantSodium CarbonateHCID 10340—
Reactanttert-butyl N-(3-aminophenyl)carbamateHCID 12877220—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57961752HCID 5796175299.1%

Reaction Steps

To a stirring solution of tert-butyl (3-aminophenyl)carbamate (2.00 g, 9.6 mmol) and triethylamine (1.40 mL, 10 mol) in dry tetrahydrofuran (27.3 mL) at 0° C. was slowly added a solution of 3-nitrobenzoyl chloride (1.87 g, 10.1 mmol) in tetrahydrofuran (7.8 mL). The resulting mixture was slowly warmed up to rt and stirred for one additional hour at rt. The reaction mixture was treated with Na2CO3 (aq). The aqueous layer was extracted with EtOAc three times. The combined organic layers were dried, filtered and concentrated to give the desired product as a white powder (3.4 g, 99%). LCMS for C18H19N3O5 (M-tBu+H)+: m/z=302.0. 1H NMR (400 MHz, CD3OD): δ 8.79 (t, J=2.0 Hz, 1H), 8.43 (ddd, J=8.0, 2.0, 1.2 Hz, 1H), 8.31 (ddd, J=6.4, 2.4, 1.2 Hz, 1H), 7.87 (t, J=2.1 Hz, 1H), 7.77 (t, J=8.0 Hz, 1H), 7.60 (ddd, J=8.0, 4.0, 2.4, 1H), 7.25 (t, J=8.0 Hz, 1H), 7.19 (d, J=1.2 Hz, 1H), 1.52 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-53227086c83d45ff954ad96a0de501db
Source noteuspto-grants-2014_10