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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927722Generated: October 31, 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/1927722

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 numberUS08183289B2
Source datasetuspto-grants-2012_05
ORD IDord-8532021433b8452c823478a2a2e1d768
Source noteuspto-grants-2012_05