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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242863Generated: October 30, 2026

Methanesulfonyl chloride → (3-o-Tolylbenzo[b]thiophen-2-yl)methyl methanesulfonate

https://huagongshe.com/reaction/242863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 68157058HCID 68157058—
SolventDichloromethaneHCID 6344—
Product(3-o-Tolylbenzo[b]thiophen-2-yl)methyl methanesulfonateHCID 8666887575%

Reaction Steps

Methanesulfonyl chloride (158 μL, 2.04 mmol) was added dropwise to a solution of (3-o-tolylbenzo[b]thiophen-2-yl)methanol (432 mg, 1.70 mmol) and DIPEA (385 μL, 2.21 mmol) in anhydrous DCM (10 mL) at RT. Stirring at RT was continued for 18 h then the reaction mixture was washed with water, then dried (Na2SO4) and concentrated in vacuo affording (3-o-tolylbenzo[b]thiophen-2-yl)methyl methanesulfonate as a brown oil (424 mg, 75%). 1H NMR (DMSO, 400 MHz): δ 8.05 (1H, d, J=8.04 Hz), 7.45-7.40 (3H, m), 7.38-7.32 (2H, m), 7.21 (1H, d, J=7.40 Hz), 7.12 (1H, d, J=7.98 Hz), 4.82 (1H, d, J=12.41 Hz), 4.76 (1H, d, J=12.41 Hz), 3.32 (3H, s), 1.99 (3H, s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-a937126a51934890aa21ba62c20187d7
Source noteuspto-grants-2014_02