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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720074Generated: October 31, 2026

1-Bromo-1-methylcyclopropane → Cyclopropylmethyl-p-toluenethiosulfonate

https://huagongshe.com/reaction/1720074

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-1-methylcyclopropaneHCID 14864946—
ReactantBenzenesulfonothioic acid, 4-methyl-, potassium salt (1:1)HCID 23662126—
SolventEthanolHCID 702—
ProductCyclopropylmethyl-p-toluenethiosulfonateHCID 8674937672.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of methylcyclopropyl bromide (4.00 g, 29.6 mmol) in ethanol (20.0 mL) was added potassium thiotosylate (10.0 g, 44.4 mmol) and the mixture heated to 90° C. for 10 h. The mixture was then quenched into a 1:1 mixture of H2O (50.0 mL) and diethyl ether (50.0 mL). The layers were separated and the organic layer washed with brine (50.0 mL). The organic layer was then dried with MgSO4 and concentrated in vacuo to yield the title compound as a solid (5.2 g, m.p. 46°-48° C.). 'H NMR (400 MHz, CDCl3) δ 7.816 (d, 2H, J=8.8 Hz), 7.308 (d, 2H, J =8.8 Hz), 2.945 (d, 2H, J=7.6 Hz), 2.451 (s, 3H), 1.010-0.933 (m, 1H), 0.592-0.545 (m, 2H), 0.236-0.197 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05504104
Source datasetuspto-grants-1996_04
ORD IDord-5a56bb9c9d3942f29a2ffffb13ce6f72
Source noteuspto-grants-1996_04