Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963945Generated: October 30, 2026

Sodium Thiosulfate → HCID 86650640, compound

https://huagongshe.com/reaction/1963945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 71742286HCID 71742286—
SolventDichloromethaneHCID 6344—
ProductHCID 86650640HCID 8665064034.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(allyloxy)-2-methylpropan-1-ol (2.37 g, 18.2 mmol) was dissolved in DCM (70 mL) and cooled to 0° C. mCPBA (77% max, 15.71 g) was added. The suspension was stirred at 0° C. for 6.5 hr before saturated NaHCO3 solution and Na2S2O3 solution were added. It was stirred at 0° C. for 15 min and the two layers were separated. The aqueous layer was extracted twice with DCM. The organic layers were combined, dried over Na2SO4 and concentrated. The resulting residue was purified on a silica gel column (heptane:EtOAc 1:0 to 1:2) to give the product as a colorless oil (910 mg, 34%). 1H NMR (400 MHz, CDCl3) δ ppm 3.65 (1H, dd, J= 11.2, 2.8 Hz), 3.47 (1H, br s), 3.31-3.41 (3H, m), 3.07-3.09 (1H, m), 2.74 (1H, t, J= 4.8 Hz), 2.63-2.65 (1H, m), 1.12 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415381B2
Source datasetuspto-grants-2013_04
ORD IDord-c7ada6231fd441b69123a4f451c47649
Source noteuspto-grants-2013_04