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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1080846Generated: November 1, 2026

Dimethylformamide → Benzyl 3-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1080846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 57275154HCID 57275154—
ProductBenzyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 277657787%

Reaction Steps

To a solution of 2-naphthalene sulfonyl-serine (prepared in Example XII Part D) (0.78 g, 2.67 mmol) and HOBT (0.4 g, 2.93 mmol) in 11 mL DMF was added WSC (0.56 g, 2.93 mmol), followed by Part D compound (1.03 g, 2.67 mmol). After 5 minutes, NMM (0.82 mL, 5.86 mmol) was added to adjust the pH to 7.5-8.0 and the reaction stirred at room temperature for 16 hrs. The reaction mixture was partitioned between EtOAc and a sat. solution of NaHCO3 and the EtOAc layer was washed with a sat. solution of KHSO4, brine, dried over Na2SO4. The organic layer was concentrated in vacuo to give title compound (87% yield). ##STR127##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05583146
Source datasetuspto-grants-1996_12
ORD IDord-dca91c5a3b63424fb5f88d6b58e8556f
Source noteuspto-grants-1996_12