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1-Cyclooctene → 2-Trifluoromethoxy-5,6,6a,7,8,9,10,11,12,12a-decahydro-5-aza-cycloocta-[a]naphthalene-6-carboxylic acid ethyl ester

HRID 47420
Notes
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Reaction equation

HRID 47420 reaction equation
[F:1][C:2]([F:12])([F:11])[O:3][C:4]1[CH:10]=[CH:9][C:7]([NH2:8])=[CH:6][CH:5]=1.[CH2:13]([O:15][C:16](=[O:19])[CH:17]=O)[CH3:14].[CH:20]1[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH:21]=1>>[CH2:13]([O:15][C:16]([CH:17]1[NH:8][C:7]2[CH:9]=[CH:10][C:4]([O:3][C:2]([F:11])([F:12])[F:1])=[CH:5][C:6]=2[CH:21]2[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH:20]12)=[O:19])[CH3:14]
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 136091-CycloocteneHCID 70211Ethyl oxoacetateHCID 6008484-(Trifluoromethoxy)aniline

Product 1

HCID 101337972-Trifluoromethoxy-5,6,6a,7,8,9,10,11,12,12a-decahydro-5-aza-cycloocta-[a]naphthalene-6-carboxylic acid ethyl ester

Procedure

Compound 76 was prepared from 4-(trifluoromethoxy)-aniline, glyoxylic acid ethyl ester and cyclooctene by the automated process.

Sources & evidence

ORD record
ord-f65ef558ff1b43d8b187200c04483bf7
Source dataset
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06699877B2

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes