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Chlorotrimethylsilane → HCID 178470819, compound

HRID 1543880
Notes
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Reaction equation

HRID 1543880 reaction equation
[Br:26][CH2:27][C:28](=[O:29])[O:30][CH2:31][CH3:32].[CH2:34]1[O:35][CH2:36][CH2:37][CH2:38]1.[Cl:1][Si:2]([CH3:3])([CH3:4])[CH3:5].[O:6]=[C:7]1[CH2:8][CH:9]([C:19](=[O:20])[O:21][C:22]([CH3:23])([CH3:24])[CH3:25])[N:10]([C:12](=[O:13])[O:14][C:15]([CH3:16])([CH3:17])[CH3:18])[CH2:11]1.[Zn:33]>>[OH:6][C:7]1([CH2:27][C:28](=[O:29])[O:30][CH2:31][CH3:32])[CH2:8][CH:9]([C:19](=[O:20])[O:21][C:22]([CH3:23])([CH3:24])[CH3:25])[N:10]([C:12](=[O:13])[O:14][C:15]([CH3:16])([CH3:17])[CH3:18])[CH2:11]1
ParticipantsSources & evidenceReaction notes

Participants

6

Reactant 5

HCID 6397ChlorotrimethylsilaneHCID 7748Ethyl bromoacetateHCID 8028TetrahydrofuranHCID 23994ZincHCID 4110468Ditert-butyl 4-oxopyrrolidine-1,2-dicarboxylate

Product 1

HCID 178470819HCID 178470819, compound

Sources & evidence

On this pageParticipantsSources & evidenceReaction notes
ORD record
ord-350df060ea924adf93a862c3ec8ddd9c
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI
10.1039/C8SC04228D

Reaction notes

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