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

HCID 57995609, compound → HCID 57995478, compound

HRID 385414
Notes
Print preview

Reaction equation

HRID 385414 reaction equation
[CH:1]1([CH2:4][O:5][C:6]2[CH:7]=[C:8]([C:15]3([C:20]([O:22][CH2:23][CH3:24])=[O:21])[CH2:19][CH2:18][CH2:17][CH2:16]3)[CH:9]=[CH:10][C:11]=2[N+:12]([O-])=O)[CH2:3][CH2:2]1>CO>[NH2:12][C:11]1[CH:10]=[CH:9][C:8]([C:15]2([C:20]([O:22][CH2:23][CH3:24])=[O:21])[CH2:19][CH2:18][CH2:17][CH2:16]2)=[CH:7][C:6]=1[O:5][CH2:4][CH:1]1[CH2:2][CH2:3]1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 57995609HCID 57995609, compound

Product 1

HCID 57995478HCID 57995478, compoundYield 82.4%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a stirred solution of ethyl 1-(3-(cyclopropylmethoxy)-4-nitrophenyl)cyclopentanecarboxylate (10 g), in dry MeOH (100 mL) Pd (OH)2 (2 g) was added and the mixture was reduced under an atmosphere of H2 for 6 h at room temperature. The mixture was filtered through a pad of Celite™, washing with MeOH. The combined filtrates were concentrated under reduced pressure to yield ethyl 1-(4-amino-3-(cyclopropylmethoxy)phenyl)cyclopentanecarboxylate (7.5 g) as a thick liquid.

Workup

  1. filtrationThe mixture was filtered through a pad of Celite™
  • washwashing with MeOH
  • concentrationThe combined filtrates were concentrated under reduced pressure
  • Sources & evidence

    ORD record
    ord-dcba4ea7ecfd4aab8497e0276417055e
    Source dataset
    uspto-grants-2013_02
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08367863B2

    Reaction notes

    Loading…

    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes