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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366465Generated: October 25, 2026

3-Methyl-3-buten-1-ol → HCID 23289305, compound

https://huagongshe.com/reaction/366465

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methyl-3-buten-1-olHCID 12988—
ReactantSodium HydroxideHCID 14798—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 23289308HCID 23289308—
SolventDichloromethaneHCID 6344—
ProductHCID 23289305HCID 2328930563%

Reaction Steps

2-Methyl-7-hydroxybenzothiazoie was alkylated with 3-methyl-3-buten-1-ol according to Method VI. The product of this alkylation (0.30 g, 1.28 mmol) was dissolved in CH2Cl2 at about 0° C. to which was then added a solution of m-chloroperbenzoic acid (0.95 g, 5.53 mmol) in CH2Cl2. The reaction was allowed to warm to room temperature and after about 0.5 h the reaction was complete. 1N NaOH was added, the layers separated and the organic layer was washed with additional 1N NaOH and H2O. The organic layer was then dried over MgSO4 and the solvent was removed by rotary evaporation to give the title compound (0.20 g, 63%) as a yellow oil which was used in subsequent reactions without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130217
Source datasetuspto-grants-2000_10
ORD IDord-9f5820d817c84634b329b7474379812f
Source noteuspto-grants-2000_10