HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1425671Generated: October 25, 2026
Water → 3-(4,5-Dimethoxy-2-nitro-benzyloxycarbonylamino)-butyric acid
https://huagongshe.com/reaction/1425671
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Beta-Aminobutyric Acid | HCID 10932 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ((Nitroveratryl)oxy)chlorocarbamate | HCID 3084878 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(4,5-Dimethoxy-2-nitro-benzyloxycarbonylamino)-butyric acid | HCID 59336635 | 36% |
Reaction Steps
3-Amino-butyric acid (147 mg, 1.43 mmol) was mixed with water (10 mL), dioxane (10 mL) and 2 M NaOH (10 mL). The mixture was cooled to 0° C. and treated with Nvoc-Cl (1.58 mmol). 2 M NaOH was added in small portions (8×1.25 mL) during 75 minutes. The cooling bath was removed and the reaction mixture was left at room temperature o/n. Water (30 mL) was added and the mixture was filtered. The aqueous phase was adjusted to pH=4 with 2 M HCl (aq.) and extracted with diethyl ether (3×50 mL). The solid was dissolved in water (50 mL) and diethyl ether (50 mL). The combined organic phases were dried over MgSO4 and evaporated in vacuo affording 176 mg (36%) pure 3-(4,5-dimethoxy-2-nitro-benzyloxycarbonylamino)-butyric acid. 1H-NMR (CDCl3): 7.72 (s, 1H), 7.02 (s, 1H), 5.51 (s, 2H), 5.40-5.30 (br s, 1H), 4.15 (m, 1H), 3.96 (s, 3H), 3.92 (s, 3H), 2.60 (d, 2H), 1.31 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08932992B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-071bd14078eb4220a24a4fb46d18f234 |
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| Source note | uspto-grants-2015_01 |
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