HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Iodoethane → Ethyl 1-Boc-3-ethylpiperidine-3-carboxylate

HRID 383893
Notes
Print preview

Reaction equation

HRID 383893 reaction equation
[CH2:1]([C:3]1([C:16]([O-:18])=[O:17])[CH2:8][CH2:7][CH2:6][N:5]([C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH2:4]1)[CH3:2].[CH2:19](I)[CH3:20]>>[CH2:1]([C:3]1([C:16]([O:18][CH2:19][CH3:20])=[O:17])[CH2:8][CH2:7][CH2:6][N:5]([C:9]([O:11][C:12]([CH3:14])([CH3:13])[CH3:15])=[O:10])[CH2:4]1)[CH3:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 6340IodoethaneHCID 756921533-Ethyl-1-[(2-methylpropan-2-yl)oxycarbonyl]piperidine-3-carboxylate

Product 1

HCID 68429349Ethyl 1-Boc-3-ethylpiperidine-3-carboxylate

Procedure

The target was synthesized as in Production Example 11(1), using 1-tert-butyl 3-ethylpiperidine-1,3-dicarboxylate and ethyl iodide as the raw material.

Workup

  1. customThe target was synthesized as in Production Example 11(1)

Sources & evidence

ORD record
ord-ced3c0fe4ffe4b6798531c68d940d563
Source dataset
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08367698B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes