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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium DithioniteHCID 24489—
ReactantBenzyl 4-(benzyloxy)-5-methoxy-2-nitrobenzoateHCID 10894498—
SolventWaterHCID 962—
ProductBenzyl 2-amino-4-(benzyloxy)-5-methoxybenzoateHCID 11057568—

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163926B2
Source datasetuspto-grants-2012_04
ORD IDord-c00a9611eef54111b70f39a2ec882320
Source noteuspto-grants-2012_04