HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823924Generated: October 30, 2026
Water → 4-tert-Butoxycarbonylamino-2-(3,4-dichlorophenyl)-butyric acid
https://huagongshe.com/reaction/1823924
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 4-Tert-butoxycarbonylamino-2-(3,4-dichlorophenyl)-butyric acid methyl ester | HCID 23570951 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-tert-Butoxycarbonylamino-2-(3,4-dichlorophenyl)-butyric acid | HCID 22147953 | 98% |
Reaction Steps
To a solution of 4-tert-butoxycarbonylamino-2-(3,4-dichlorophenyl)-butyric acid methyl ester (12.3 g, 34 mmol) in THF (80 mL)/water (20 mL) was added lithium hydroxide (1.63 g, 68 mmol) at 0° C. The reaction mixture was allowed to warm to room temperature and stirred overnight. The reaction mixture was concentrated and the residue diluted with water. After extraction with EtOAc, the aqueous phase was acidified to pH 5 by the addition of 2M aqueous hydrochloric acid solution. The aqueous phase was extracted with EtOAc and the extracts dried over magnesium sulfate. Concentration gave the title compound as a pale brown foam (11.54 g, 98%); 1H NMR (400 MHz, DMSO) δ 1.35 (9H, s), 1.74–1.81 (1H, m), 2.03–2.10 (1H, m), 2.81 (2H, m), 3.61 (1H, t), 6.86 (1H, m), 7.28 (1H, dd), 7.54 (1H, dd), 7.59 (1H, d), 12.60 (1H, brs); MS (ES−) m/e=346.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07041687B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-abcf6e0a239345a1bae17a3dd71407b6 |
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| Source note | uspto-grants-2006_05 |
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