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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388806Generated: October 30, 2026

Acetic Acid → 4-[4-(Tert-butoxycarbonylamino-methyl)piperidin-1-ylmethyl]-piperidine-1-carboxylic acid methyl ester

https://huagongshe.com/reaction/388806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTert-butyl (piperidin-4-ylmethyl)carbamateHCID 723429—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 4-formylpiperidine-1-carboxylateHCID 45123041—
SolventDichloromethaneHCID 6344—
Product4-[4-(Tert-butoxycarbonylamino-methyl)piperidin-1-ylmethyl]-piperidine-1-carboxylic acid methyl esterHCID 6681090370.5%

Reaction Steps

To a solution of 4-tert-butoxycarbonylaminomethylpiperidine (3.62 g, 16.9 mmol) in dichloromethane (100 mL) was added 4-formylpiperidine-1-carboxylic acid methyl ester (2.89 g, 16.9 mmol) and acetic acid (0.96 mL). The mixture was stirred at room temperature for 10 min prior to the addition of sodium triacetoxyborohydride (5.4 g, 25.5 mmol). The final mixture was stirred at room temperature for 1 h. The reaction was terminated by adding saturated sodium bicarbonate solution (50 mL). The mixture was extracted with dichloromethane (100 mL), and the organic layer was dried over MgSO4. Evaporation of the organic solution afforded a pale yellow oily residue. It was purified by flash silica column chromatography (CH2Cl2 to 5% MeOH/CH2Cl2), yielding the title intermediate (4.4 g). (m/z): [M+H]+ calcd for C19H35N3O4 370.27. found 370.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377964B2
Source datasetuspto-grants-2013_02
ORD IDord-a69ba8754749462c87cd032ed81ca4a8
Source noteuspto-grants-2013_02