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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349805Generated: October 26, 2026

tert-Butylsulfinamide, (S)-(-)- → (S)-2-Methyl-propane-2-sulfinic Acid ((3S)-1,3-dimethyl-pentylidene)-amide

https://huagongshe.com/reaction/349805

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
Reactant(S)-4-methyl-hexan-2-oneHCID 12208763—
CatalystTitanium tetraethoxideHCID 76524—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product(S)-2-Methyl-propane-2-sulfinic Acid ((3S)-1,3-dimethyl-pentylidene)-amideHCID 8659795663.4%

Reaction Steps

A mixture of (S)-4-methyl-hexan-2-one (1.6 g, 14 mmol), (S)-2-methyl-propane-2-sulfinic acid amide (1.7 g, 14 mmol) and titanium(IV)ethoxide (6.4 g, 28 mmol) in THF (30 mL) was refluxed for 10 hours. Then the reaction mixture was poured into brine (150 mL). The mixture was filtered. The filtrate was extracted by EtOAc (3×70 mL). The EtOAc phase was removed under reduce pressure and the residue was purified by a silica gel column (Hexane/EtOAc 3:1) to give the titled compound (1.93 g, 63% yield) as a colorless oil: 1H NMR (CDCl3) δ 2.24 (m, 2H), 2.27 (s, 3H), 1.85 (m, 1H), 1.22 (m, 2H), 1.20(s, 9H), 0.85 (m, 6H); MS (APCl) (M+1)+ 218.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179934B2
Source datasetuspto-grants-2007_02
ORD IDord-683026977ad74c3582d1a6bb62307944
Source noteuspto-grants-2007_02