HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686996Generated: November 3, 2026
Lithium Hydroxide → 2-(2-Tert-butoxycarbonylaminoethylamino)-6-nitro-benzoic acid
https://huagongshe.com/reaction/1686996
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 2-(2-Tert-butoxycarbonylaminoethylamino)-6-nitro-benzoic acid methylester | HCID 67264259 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | 2-(2-Tert-butoxycarbonylaminoethylamino)-6-nitro-benzoic acid | HCID 67264612 | 96% |
Reaction Steps
To a solution of 2-(2-tert-butoxycarbonylaminoethylamino)-6-nitro-benzoic acid methylester (0.26 g, 0.00077 mol) in THF-water (3:1, 20 mL) under nitrogen was added lithium hydroxide (0.14 g, 0.00326 mol) as a solid in one portion. The reaction mixture was heated at 50° C. for 5 h then cooled to room temperature overnight. The mixture was diluted with ethyl acetate (10 mL) and washed with 10% aqueous HCl, water, and brine. The organic phase was dried over magnesium sulfate, filtered and concentrated in vacuo to a yellow oil which was purified by ISCO chromatography on silica gel using 15-50% ethyl acetate-hexane to give product as a pale yellow oil 2-(2-tert-butoxycarbonylaminoethylamino)-6-nitro-benzoic acid (0.24 g, 96%). 1H NMR (400 MHz, CDCl3) δ 11.8 (s, 1H), 7.57 (t, 1H, J=7.8 Hz), 7.05 (d, 1H, J=7.8 Hz), 6.81 (d, 1H, J=7.8 Hz), 6.73 (s, 1H), 4.5 (s, 1H), 3.47 (m, 2H), 3.19 (m, 2H), 1.47 (s, 9H); MS (m/e) 326 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08148391B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-8ffa6834cad44c72b61d13cbd46dc1fd |
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| Source note | uspto-grants-2012_04 |
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