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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760395Generated: November 3, 2026

Chlorodiphenylmethane → N-diphenylmethyloxy-tert-butyl-(dimethyl-tert-butylamino-carbonyl-methyl)-amine

https://huagongshe.com/reaction/1760395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorodiphenylmethaneHCID 7035—
ReactantTert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-hydroxylamineHCID 22182216—
ProductN-diphenylmethyloxy-tert-butyl-(dimethyl-tert-butylamino-carbonyl-methyl)-amineHCID 2356382462.7%

Reaction Steps

The compound is prepared in analogy to example A13 from tert-butyl-(dimethyl-tert-butylaminocarbonyl-methyl)-hydroxylamine and diphenylmethylchloride in 62.7% yield as colorless crystals, m.p. 89-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06841703B2
Source datasetuspto-grants-2005_01
ORD IDord-1e151d4d8cc3405ab553a60aeff30661
Source noteuspto-grants-2005_01