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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356510Generated: October 30, 2026

D-1,4-Dithiothreitol → Dimethyl-sulfamic acid 5-tert-butyl-4-mercapto-2-methyl-phenyl ester

https://huagongshe.com/reaction/356510

Reaction equation

Participants

RoleNameHCIDCharge
ReactantD-1,4-DithiothreitolHCID 446094—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantDimethyl-sulfamic acid 5-tert-butyl-2-methyl-4-thiocyanato-phenyl esterHCID 10496539—
SolventEthanolHCID 702—
ProductDimethyl-sulfamic acid 5-tert-butyl-4-mercapto-2-methyl-phenyl esterHCID 10662229—

Reaction Steps

To a round bottom flask equipped with a magnetic stirrer and condenser were added 1.1 g (3.3 mmol) of dimethyl-sulfamic acid 5-tert-butyl-2-methyl-4-thiocyanato-phenyl ester (prepared in Example SSS), dithiothreitol (1.29 g, 8.35 mmol), EtOH (40 mL), and 0.02M KH2PO4 buffer solution (5 mL), respectively. The reaction was refluxed overnight. The mixture was then quenched with H2O (250 mL) and extracted with a 1:1 mixture of hexanes:Et2O. The organic layer was again washed with H2O and brine, dried (MgSO4) and concentrated. The residue was dried under high vacuum to yield the title compound. 1H NMR (CDCl3) δ 1.45 (s, 9 H), 2.25 (s, 3 H), 3.02 (s, 6 H), 3.57 (s, 1 H), 7.01 (s, 1 H), 7.28 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834506
Source datasetuspto-grants-1998_11
ORD IDord-0fc603a7f9a749d28b0d169bb4db6176
Source noteuspto-grants-1998_11