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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964487Generated: October 30, 2026

Citric Acid → 3-({[(Tert-butoxy)carbonyl]amino}methyl)-5-nitrobenzoic acid

https://huagongshe.com/reaction/964487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantSodium HydroxideHCID 14798—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantMethyl 3-(aminomethyl)-5-nitrobenzoateHCID 19077132—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product3-({[(Tert-butoxy)carbonyl]amino}methyl)-5-nitrobenzoic acidHCID 1907713488%

Reaction Steps

A solution of methyl 5-nitro-3-aminomethybenzoate (1980 mg, 9.4 mmol) in 1N NaOH (28 mL, 28 mmol) and tert-BuOH (20 mL) was stirred at r.t. for 10 hours and then added BOC2O (4100 mg, 18.8 mmol) and stirred for 17 hours. The reaction mixture was added hexanes (50 mL) and water (50 mL). The aqueous layer was acidified with 5% citric acid aq. and extracted with CH2 Cl2 (2×70 mL). The CH2Cl2 layers were combined and washed with water (50 mL). The organic layer was evaporated to give the desired compound (2450 mg, 88%): 1H NMR (300 MHz, DMSO-d6) δ 13.725 (s, 1H), 8.476 (s, 1H), 8.307 (s, 1H), 8.216 (s, 1H), 7.639 (t, J=5.7 Hz, 1H), 4.398 (d, J=5.7 Hz, 2H), 1.385 (s, 9H); 13C NMR (300 MHz, DMSO-d6) δ 165.5, 155.9, 147.9, 143.5, 133.6, 132.5, 125.4, 122.2, 78.3, 42.6, 28.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05770380
Source datasetuspto-grants-1998_06
ORD IDord-991de5e9c97e490b943c2a4013aaa6de
Source noteuspto-grants-1998_06