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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | Methyl 3-(aminomethyl)-5-nitrobenzoate | HCID 19077132 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 3-({[(Tert-butoxy)carbonyl]amino}methyl)-5-nitrobenzoic acid | HCID 19077134 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05770380 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-991de5e9c97e490b943c2a4013aaa6de |
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| Source note | uspto-grants-1998_06 |
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