Ethanol → HCID 86596485, compound

HRID 1247695Notes

Reaction equation

HRID 1247695 reaction equation
[CH2:1]([OH:3])C.[S:4](=[O:8])(=[O:7])([OH:6])[OH:5].[CH:9]([Cl:12])([Cl:11])[Cl:10]>>[CH:9]([Cl:12])([Cl:11])[Cl:10].[CH3:1][OH:3].[S:4](=[O:6])(=[O:5])([OH:8])[OH:7]

Participants

4

Procedure

A colorless solid (0.078 g, yield: 82.1%) was obtained through a reaction conducted as in example 2 except that the reactants were replaced by the compound (117) prepared in example 17 (0.1 g), ethanol (66.6 mL), chloroform (100 mL), and sulfuric acid (36 N, 0.3 mL), and the reaction time was adjusted to 96 hours. IR analysis of the product revealed the existence of an absorption band that suggested an acetoxy group at 1740 cm−1. 1H-NMR analysis revealed the product consists of a compound (138) and the compound (117) (content of compound (138): 90.1 mol %).

Sources & evidence

ORD record
ord-3857d174708b463a88ed5c4acfc57d3d
Source dataset
uspto-grants-2006_10
Patent number
US07129370B2

Reaction notes

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