HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538901Generated: October 30, 2026
Water → Benzyl 2-amino-4-(benzyloxy)-5-methoxybenzoate
https://huagongshe.com/reaction/538901
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Benzyl 4-(benzyloxy)-5-methoxy-2-nitrobenzoate | HCID 10894498 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Benzyl 2-amino-4-(benzyloxy)-5-methoxybenzoate | HCID 11057568 | — |
Reaction Steps
Benzyl 4-(benzyloxy)-5-methoxy-2-nitrobenzoate (77 g) was dissolved in acetonitrile (882 ml). Sodium dithionite (160.5 g) was added to the solution and the temperature adjusted to 25° C. Water (588 ml) was then added, maintaining the temperature at 25° C. The pH was maintained at 6 using 8.8 M sodium hydroxide during the reduction. The slurry was then heated to 65° C. and the lower aqueous phase was removed. Concentrated hydrochloric acid (35% w/w, 7.25 ml) was then added. The slurry was allowed to cool to 40° C. and then to 20° C. Sodium hydroxide solution (47% w/w, 12.4 ml) was added and the slurry cooled to 0° C. The product (benzyl 2-amino-4-(benzyloxy)-5-methoxybenzoate) was isolated by filtration, washed with water (2×196 ml) and then dried at 40° C. under vacuum. Yield: 66.2 g, 92.4%; NMR Spectrum (CDCl3) 3.8 (s, 3H), 5.1 (s, 2H), 5.3 (s, 2H), 6.2 (s, 1H), 7.3-7.4 (m, 10H); Mass Spectrum (M+H)+=364.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865899B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-c8cc3ac0360a4a57b2ae75af08756405 |
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| Source note | uspto-grants-2014_10 |
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