Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585869Generated: November 1, 2026

Dimethyl Sulfide → HCID 15428582, compound

https://huagongshe.com/reaction/1585869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 15428581HCID 15428581—
SolventDichloromethaneHCID 6344—
ProductHCID 15428582HCID 15428582—

Reaction Steps

A solution of NBS (1.59 g, 8.94 mmol) and CH2Cl2 was cooled to 0°. To this solution (under Ar) was added Me2S (10.72 mmol, 0.78 mL) via syringe. This mixture was then cooled to -20° and added to a solution of the benzyl alcohol from Step 2 (1.2 g, 5.96 mmol) in CH2Cl2 via pipette. The reaction mixture was warmed to 0° and stirred for several hours. The residue was poured into ice water and extracted with CH2Cl2 (3×). The organic layers were combined, washed with brine, dried (MgSO4), filtered and concentrated to give the title compound as a yellow solid, which will be used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05939439
Source datasetuspto-grants-1999_08
ORD IDord-9ba8d12b1f4d434f88795699b58aa633
Source noteuspto-grants-1999_08