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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554824Generated: October 31, 2026

Sodium borohydride → Tert-butyl 4-(1-aminopropyl)-2-nitrobenzoate

https://huagongshe.com/reaction/554824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantAzane;hydrateHCID 12896473—
ReactantTert-butyl 2-nitro-4-propionylbenzoateHCID 66935244—
CatalystHCID 178460666HCID 178460666—
SolventEthanol, reaction products with ammonia, distn. residuesHCID 22020343—
ProductTert-butyl 4-(1-aminopropyl)-2-nitrobenzoateHCID 67461906—

Reaction Steps

Tert-butyl 2-nitro-4-propionylbenzoate (9.2 g) was suspended in 2N ammonia/ethanol solution (81 ml), then tetraisopropoxytitanium (18.7 ml) was added at room temperature and the mixture was stirred at that temperature for 6 hours. Next, sodium borohydride (1.8 g) was added to the mixture, and the resulting mixture was stirred at that temperature for 16 hours. Then 2.1N ammonia water (81 ml) and Celite (9g) were added to the reaction solution and the inspluble materials were filtered off and washed with water and ethyl acetate. The filtrate was concentrated in vacuo, then a 5N aqueous sodium hydroxide solution and ethyl acetate were added to the obtained residue. The separated organic layer was concentrated in vacuo, then the obtained residue was purified by silica gel column chromatography to obtain the title compound (7.6 g) as an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08049006B2
Source datasetuspto-grants-2011_11
ORD IDord-9fdd327512614da6b1a8fe56fa00f978
Source noteuspto-grants-2011_11