HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697849Generated: October 30, 2026
Acetonitrile → Benzyl 2-amino-4-(benzyloxy)-5-methoxybenzoate
https://huagongshe.com/reaction/1697849
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Reactant | Benzyl 4-(benzyloxy)-5-methoxy-2-nitrobenzoate | HCID 10894498 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl 2-amino-4-(benzyloxy)-5-methoxybenzoate | HCID 11057568 | — |
Reaction Steps
Benzyl 4-(benzyloxy)-5-methoxy-2-nitrobenzoate (90 g) was charged to acetonitrile (660 g). 85% Sodium dithionite (75 g) was added to the solution and the temperature adjusted to 20° C. Water (516 g) was then added, maintaining the temperature at 20° C. The slurry was then heated to 65° C. and stirred for 30 minutes. Sodium dithionite (75 g) was added and the mixture stirred for another 30 minutes. The lower aqueous phase was removed. Concentrated hydrochloric acid (33% w/w, 12.48 g) was then added to adjust to a pH of <1. The suspension is held for 1 hour. The slurry was cooled to 20° C. over 30 minutes. Sodium hydroxide solution (20% w/w, 59.29 g) was added to give a pH of 10. The slurry was cooled to 0° C. and stirred for one hour. The product (benzyl 2-amino-4-(benzyloxy)-5-methoxybenzoate) was isolated by filtration, washed twice with water (2×222 ml) and then dried at 60° C. under vacuum. Yield: 78.81 g, 95%; 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 | US08163926B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-c00a9611eef54111b70f39a2ec882320 |
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| Source note | uspto-grants-2012_04 |
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