HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445448Generated: October 31, 2026
Water → 2-[2-(Tert-butoxycarbonylamino)ethoxy]-4-methoxybenzoic acid
https://huagongshe.com/reaction/1445448
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Methyl 2-[2-(tert-butoxycarbonylamino)ethoxy]-4-methoxybenzoate | HCID 68530686 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[2-(Tert-butoxycarbonylamino)ethoxy]-4-methoxybenzoic acid | HCID 68534273 | 91% |
Reaction Steps
Methyl 2-[2-(tert-butoxycarbonylamino)ethoxy]-4-methoxybenzoate (1.0 g, 3.07 mmol) was suspended in 20 ml of 3:1 tetrahydrofuran (THF):water, then chilled on ice for 30 min with stirring. Next there was added solid lithium hydroxide monohydrate (284 mg, 6.76 mmol) to the suspension, and the mixture was stirred at room temperature for 20 h at which time TLC (50:50:1 hexanes:EtOAc:AcOH) showed complete consumption of starting ester. The slurry was diluted with water (50 ml), washed twice with ethyl ether, then the aqueous layer was acidified to pH 2 with 1 N NaHSO4 to yield a heavy white slurry. The slurry was extracted twice with EtOAc, then the EtOAc layers were combined, washed with brine, dried over Na2SO4, and concentrated in vacuo to provide 2-[2-(tert-butoxycarbonylamino)ethoxy]-4-methoxybenzoic acid (870 mg, 91%) as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07666866B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-293df42beaf144a8ae761a683e0d7f93 |
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| Source note | uspto-grants-2010_02 |
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