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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037946Generated: November 2, 2026

Water → HCID 87383933, compound

https://huagongshe.com/reaction/1037946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactanttert-Butylsulfinamide, (S)-(-)-HCID 11355477—
Reactanttert-Butyl 5-formylthiophene-2-carboxylateHCID 21473735—
CatalystTitanium isopropoxideHCID 11026—
SolventDichloromethaneHCID 6344—
ProductHCID 87383933HCID 8738393387%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 500-mL round-bottom flask was added (S)-(−)-2-methyl-2-propanesulfinamide (1.62 g, 13.4 mmol), and tert-butyl 5-formylthiophene-2-carboxylate (2.37 g, 11.2 mmol), and DCM (100 mL). The mixture was cooled to 0° C., then titanium tetraisopropoxide (19.8 mL, 67.0 mmol) was added. After the solution was warmed to rt and stirred for 16 h, the reaction mixture was diluted with DCM (200 mL). To the flask was added water (19.8 mL) slowly. The mixture was vigorously stirred at rt for 30 min, then filtered through a pad of Celite. The filtrate was concentrated to give a solid. Purification via flash chromatography (hexanes to 10% EtOAc-hexanes) afforded (S,E)-tert-butyl 5-((tert-butylsulfinylimino)methyl)thiophene-2-carboxylate (3.07 g, 87%) as a white solid. 1H NMR (CDCl3, 400 MHz) δ 8.65 (s, 1H), 7.72 (d, J=4.0 Hz, 1H), 7.65 (d, J=3.8 Hz, 1H), 1.58 (s, 9H), 1.24 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546588B2
Source datasetuspto-grants-2013_10
ORD IDord-8af38ae89c3a4407823c8f811cf8c4ae
Source noteuspto-grants-2013_10