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26309-99-9

26309-99-9 Structure

26309-99-9 Structure
IdentificationBack Directory
[Name]

6-ChloroMethyl-2,3-dihydro-benzo[1,4]dioxine
[CAS]

26309-99-9
[Synonyms]

4]dioxine
6-(chloroMethyl)-2
6-ChloroMethyl-2,3-dihydro-benzo[1,4]dioxine
6-(Chloromethyl)-2,3-dihydro-1,4-benzodioxin
6-(chloromethyl)-2,3-dihydro-1,4-benzodioxine
1,4-Benzodioxin, 6-(chloromethyl)-2,3-dihydro-
[Molecular Formula]

C9H9ClO2
[MDL Number]

MFCD04362149
[MOL File]

26309-99-9.mol
[Molecular Weight]

184.62
Chemical PropertiesBack Directory
[Boiling point ]

125-125 °C(Press: 0.07 Torr)
[density ]

1.264±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
Hazard InformationBack Directory
[Synthesis]

2,3-DIHYDRO-1,4-BENZODIOXIN-6-YLMETHANOL

39270-39-8

6-ChloroMethyl-2,3-dihydro-benzo[1,4]dioxine

26309-99-9

General procedure for the synthesis of 6-(chloromethyl)-2,3-dihydrobenzo[b][1,4]dioxazine from benzodioxane-6-methanol: A mixture of (2,3-dihydrobenzo[1,4]dioxin-6-yl)methanol (10.6 g) with SOCl2 (10 mL) was stirred at room temperature for 10 min, followed by slow pouring of the reaction mixture into ice water. The organic layer was separated and the aqueous phase was extracted with dichloromethane (50 mL x 3). All organic layers were combined and washed sequentially with saturated NaHCO3 solution, water and brine, dried over Na2SO4 and concentrated to dryness under reduced pressure to afford 6-(chloromethyl)-2,3-dihydrobenzo[1,4]dioxin (12 g, 88% yield). The product did not require further purification and could be used directly in the next step of the reaction.

[References]

[1] Patent: US2011/98311, 2011, A1
[2] Tetrahedron, 2001, vol. 57, # 39, p. 8297 - 8303
[3] Patent: US2007/244159, 2007, A1. Location in patent: Page/Page column 103-104
[4] Patent: US2015/231142, 2015, A1. Location in patent: Paragraph 1628
[5] Patent: WO2008/141119, 2008, A2. Location in patent: Page/Page column 76-77
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39270-39-8 29668-44-8 80985-34-8 116939-11-8 79440-34-9