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Triethylamine → 1-Methanesulfonyl-piperidine-4-carboxylic acid benzyl ester

HRID 556303
Notes
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Reaction equation

HRID 556303 reaction equation
Cl.[CH2:2]([O:9][C:10]([CH:12]1[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]1)=[O:11])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C(N(CC)CC)C.[CH3:25][S:26](Cl)(=[O:28])=[O:27]>CN(C=O)C.O>[CH2:2]([O:9][C:10]([CH:12]1[CH2:17][CH2:16][N:15]([S:26]([CH3:25])(=[O:28])=[O:27])[CH2:14][CH2:13]1)=[O:11])[C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 68664822Benzyl piperidine-4-carboxylate hydrochloride

Product 1

HCID 574280631-Methanesulfonyl-piperidine-4-carboxylic acid benzyl esterYield 78%

Reagents, catalysts & solvents 2

HCID 962WaterSolvent
HCID 6228
Dimethylformamide
Solvent

Procedure

Piperidine-4-carboxylic acid benzyl ester, hydrochloride salt (1 g, 3.9 mmol, 1e.) from step 3, was dissolved in DMF (15 ml), Triethylamine (0.55 ml, 4 mmol, 1 eq.) and methanesulfonylchloride were added. The mixture was stirred for 1 h at room temperature, then was poured in water (20 ml). The aqueous solution was extracted with Ethyl Acetate (90 ml) and the organic layer was dried over anhydrous sodium sulfate, evaporated under reduced pressure to give a colourless oil. Yield 78%, 0.9 g.

Workup

  1. extractionThe aqueous solution was extracted with Ethyl Acetate (90 ml)
  2. dry with materialthe organic layer was dried over anhydrous sodium sulfate
  3. customevaporated under reduced pressure
  4. customto give a colourless oil

Sources & evidence

ORD record
ord-5dd2ee062b1c4a19b42dd555a4568765
Source dataset
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08058262B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes