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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453491Generated: October 30, 2026

Methyl 4-(4-(2-tert-butoxy-2-oxoethyl)-2-cyanophenoxy)benzoate → Methyl 4-(2-(aminomethyl)-4-(2-tert-butoxy-2-oxoethyl)phenoxy)benzoate

https://huagongshe.com/reaction/453491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(4-(2-tert-butoxy-2-oxoethyl)-2-cyanophenoxy)benzoateHCID 68466372—
CatalystNickelHCID 935—
SolventAmmonia methanolHCID 21705897—
ProductMethyl 4-(2-(aminomethyl)-4-(2-tert-butoxy-2-oxoethyl)phenoxy)benzoateHCID 6846483174%

Reaction Steps

The product of step A (2.5 g, 6.80 mmol) was diluted with 7N ammonia/methanol (30 mL) followed by the addition of Raney Nickel (0.0583 g, 0.680 mmol). The reaction mixture was purged three times with hydrogen and stirred for 12 hours. The reaction mixture was then filtered through a GF/F filter and concentrated. The residue was purified using a biotage 40M column eluting with methylene chloride:MeOH:NH4OH (90:9:1) to yield methyl 4-(2-(aminomethyl)-4-(2-tert-butoxy-2-oxoethyl)phenoxy)benzoate (1.87 g, 74.0% yield) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492437B2
Source datasetuspto-grants-2013_07
ORD IDord-9d42f0ee77874b4fb9c2624419ee2c57
Source noteuspto-grants-2013_07