4-Aminotetrahydro-2H-thiopyran 1,1-dioxide
4-Aminotetrahydro-2H-thiopyran 1,1-dioxide Basic information
- Product Name:
- 4-Aminotetrahydro-2H-thiopyran 1,1-dioxide
- Synonyms:
-
- 2H-Thiopyran-4-amine,tetrahydro-,1,1-dioxide(9CI)
- Tetrahydro-2H-thiopyran-4-amine 1,1-dioxide
- (1,1-dioxidotetrahydro-2H-thiopyran-4-yl)amine(SALTDATA: HCl)
- 2H-Thiopyran-4-aMine, tetrahydro-, 1,1-dioxide
- 1,1-Dioxo-tetrahydrothiopyran-4-aMine
- (1,1-diketothian-4-yl)amine hydrochloride
- 4-Aminotetrahydro-2H-thiopyran 1,1-dioxide
- 1,1-dioxothian-4-amine
- CAS:
- 210240-20-3
- MF:
- C5H11NO2S
- MW:
- 149.21
- Product Categories:
-
- AMINEPRIMARY
- Mol File:
- 210240-20-3.mol
4-Aminotetrahydro-2H-thiopyran 1,1-dioxide Chemical Properties
- Boiling point:
- 339.7±35.0 °C(Predicted)
- Density
- 1.237
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- pka
- 8.32±0.20(Predicted)
- Appearance
- Off-white to light yellow Solid
4-Aminotetrahydro-2H-thiopyran 1,1-dioxide Usage And Synthesis
Synthesis
99586-63-7
210240-20-3
General procedure for the synthesis of 4-aminotetrahydro-2H-thiopyran 1,1-dioxide from the compound (CAS:99586-63-7): to a stirred methanolic solution of compound 4.3 (0.14 g, 0.85 mmol) was added Raney Ni catalyst and the resulting mixture was stirred and reacted for 3 hours at room temperature in hydrogen atmosphere. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was filtered and the methanolic filtrate was concentrated under reduced pressure to afford the target product 4-aminotetrahydro-2H-thiopyran 1,1-dioxide (Compound 4.4, 0.10 g, 78% yield).
References
[1] Patent: US2009/82423, 2009, A1. Location in patent: Page/Page column 24
[2] Journal of the American Chemical Society, 1955, vol. 77, p. 3866,3867
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