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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003865Generated: November 2, 2026

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

https://huagongshe.com/reaction/1003865

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 0.02 M 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 numberUS06046355
Source datasetuspto-grants-2000_04
ORD IDord-1b1a3e2398be4d3290266b1c0588f14b
Source noteuspto-grants-2000_04