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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429826Generated: October 31, 2026

1-(p-Methoxyphenyl)-2-propanone → HCID 18352986, compound

https://huagongshe.com/reaction/429826

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(p-Methoxyphenyl)-2-propanoneHCID 31231—
Reactant1-Boc-4-(aminomethyl)piperidineHCID 736817—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductHCID 18352986HCID 1835298682.5%

Reaction Steps

A solution of sodium cyanoborohydride (1.07 grams, 17 mmole), 4-aminomethyl-1-(tert-butoxycarbonyl)piperidine (3.0 grams, 14.3 mole) and 1-(4-methoxyphenyl)propan-2-one (2.35 grams, 14.31 mmole) in methanol (50 ml) was stirred at 22° C. for 17 hours. The mixture was concentrated under reduced pressure and the residue was partitioned between ethyl acetate and water. The dried (anhydrous magnesium sulfate) organic phase was concentrated under reduced pressure to leave N-[2-(4-methoxyphenyl)-1-methylethyl]-[1-(tert-butoxycarbonyl)piperidin-4-ylmethyl]amine as an oil (4.28 grams, 82%); hydrochloride, m.p. 198-199° C. (methanol/ethyl ether), M+H 391.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06319920B1
Source datasetuspto-grants-2001_11
ORD IDord-a0520b2b631b4525a2c7b2edd19a4a5f
Source noteuspto-grants-2001_11