Identification | Back Directory | [Name]
6-iodochroman-2-one | [CAS]
128651-99-0 | [Synonyms]
6-iodochroman-2-one 2H-1-BENZOPYRAN-2-ONE, 3,4-DIHYDRO-6-IODO- 3,?4-?Dihydro-?6-?iodo-?2H-?1-?benzopyran-?2-?one | [Molecular Formula]
C9H7IO2 | [MOL File]
128651-99-0.mol | [Molecular Weight]
274.06 |
Chemical Properties | Back Directory | [Melting point ]
133-134 °C | [Boiling point ]
350.8±31.0 °C(Predicted) | [density ]
1.878±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C(protect from light) | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Synthesis]
The general procedure for the synthesis of 6-iodobenzodihydropyran-2-one from hydrogenated cinnamic acid lactone was carried out as follows, with reference to literature [41] for the synthesis. In a flame-dried and argon flushed 250 cm3 two-necked round-bottomed flask equipped with a dropping funnel and an argon inlet, 5.00 g of dihydrocoumarin (15, 33.8 mmol) was dissolved in 35 cm3 dichloromethane (DCM). ICl (5.48 g, 33.8 mmol) dissolved in 35 cm3 DCM was slowly added through a dropping funnel over 15 min. The reaction was fully converted (after 20 h) and the reaction mixture was diluted with 100 cm3 DCM and washed with 0.1 M Na?S?O? solution (2 × 50 cm3). The combined aqueous phases were re-extracted with DCM (2 × 50 cm3). The combined organic layers were washed with saturated NaCl solution (1 × 200 cm3), dried over MgSO?, filtered, and the solvent was removed in vacuum. Recrystallization by DCM/cyclohexane (1/4) afforded 8.28 g (90% yield) of the product in the form of a colorless powder.16 The melting point was determined to be 134-136°C (133-134°C reported in the literature [37]); the nuclear magnetic resonance (NMR) data were in agreement with that described in the literature [41]. | [References]
[1] Monatshefte fur Chemie, 2016, vol. 147, # 3, p. 509 - 521 [2] Journal of Organometallic Chemistry, 1990, vol. 387, # 3, p. 381 - 390 |
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