3-Oxetanemethanol, 3-(1,1-dimethylethyl)- → 4-t-Butyl-1-(but-3-ynylthiomethyl)-2,6,7-trioxabicyclo[2.2.2]octane

HRID 1197361Notes

Reaction equation

HRID 1197361 reaction equation
C(SCC(O)=O)CC#C.C(C1(CO)COC1)(C)(C)C.[C:20]([C:24]12[CH2:31][O:30][C:27]([CH:32]([S:34][CH2:35][CH2:36][C:37]#[CH:38])C)([O:28][CH2:29]1)[O:26][CH2:25]2)([CH3:23])([CH3:22])[CH3:21]>>[C:20]([C:24]12[CH2:25][O:26][C:27]([CH2:32][S:34][CH2:35][CH2:36][C:37]#[CH:38])([O:28][CH2:29]1)[O:30][CH2:31]2)([CH3:23])([CH3:22])[CH3:21]

Participants

4

Reactant 3

HCID 1807403-Oxetanemethanol, 3-(1,1-dimethylethyl)-HCID 193732562-(But-3-ynylthio)acetic acidHCID 198970494-t-Butyl-1-[1-(but-3-yn-1-ylthio)ethyl]-2,6,7-trioxabicyclo[2.2.2]octane

Product 1

HCID 193733124-t-Butyl-1-(but-3-ynylthiomethyl)-2,6,7-trioxabicyclo[2.2.2]octane

Procedure

4-t-Butyl-1-(but-3-ynylthiomethyl)-2,6,7-trioxabicyclo[2.2.2]octane was prepared from 2-(but-3-ynylthio)acetic acid and 3-t-butyl-3-hydroxymethyloxetane using the methodology described in Example I. A small amount of 4-t-butyl-1-[1-(but-3-yn-1-ylthio)ethyl]-2,6,7-trioxabicyclo[2.2.2]octane was also present.

Sources & evidence

ORD record
ord-96c2cdcb046e4a5086be022917441c4d
Source dataset
uspto-grants-1992_05
Patent number
US05116862

Reaction notes

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