Acetone → (1,3-Oxazolidin-2-on-4-yl)methyl Thioacetate

Reaction equation

[C:19]([CH3:20])(=[S:21])[O-:22].[CH2:23]([N+:24]([CH2:25][CH2:26][CH2:27][CH3:28])([CH2:29][CH2:30][CH2:31][CH3:32])[CH2:33][CH2:34][CH2:35][CH3:36])[CH2:37][CH2:38][CH3:39].[CH3:40][C:41](=[O:42])[CH3:43].[c:1]1([CH3:2])[cH:3][cH:4][c:5]([S:6](=[O:7])(=[O:8])[O:10][CH2:11][CH:12]2[NH:13][C:14](=[O:17])[O:15][CH2:16]2)[cH:9][cH:18]1>>[O:10]([CH2:11][CH:12]1[NH:13][C:14](=[O:17])[O:15][CH2:16]1)[C:19]([CH3:20])=[S:21]

Participants

Reactant 4

HCID 180Acetone

HCID 16028Tetrabutylammonium

HCID 14456891(2-Oxo-1,3-oxazolidin-4-yl)methyl 4-methylbenzene-1-sulfonate

HCID 178476994HCID 178476994, compound

Product 1

HCID 21291365(1,3-Oxazolidin-2-on-4-yl)methyl Thioacetate

Sources & evidence

ORD record: ord-98cbd70c7fa3470cad1aabb69eb932e5
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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