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Home > Encyclopedia > 5-Bromo-1,2-difluoro-3-methoxybenzene

5-Bromo-1,2-difluoro-3-methoxybenzene

5-Bromo-1,2-difluoro-3-methoxybenzene structure

5-Bromo-1,2-difluoro-3-methoxybenzene 

structure
  • CAS No:

    261762-35-0

  • Formula:

    C7H5BrF2O

  • Chemical Name:

    5-Bromo-1,2-difluoro-3-methoxybenzene

  • Synonyms:

    Benzene,5-bromo-1,2-difluoro-3-methoxy-;5-Bromo-1,2-difluoro-3-methoxybenzene;5-Bromo-2,3-difluoroanisole;1-Bromo-3,4-difluoro-5-methoxybenzene

  • Categories:

    Organic Chemistry  >  Organic Fluorine Compound

Description

White crystalline powder

5-Bromo-1,2-difluoro-3-methoxybenzene Basic Attributes

223.01

223.01

-0

DTXSID30378340

2909309090

Characteristics

9.2

2.8

1.6±0.1 g/cm3

33-35°C

193.7°C at 760 mmHg

84.6±10.2 °C

1.500

Room temperature.

0.639mmHg at 25°C

Safety Information

IRRITANT

36/37/38

26-36

Xi

Irritant

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 6 companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

5-Bromo-1,2-difluoro-3-methoxybenzene Use and Manufacturing

To a solution of 81 (1.5 g, 7.1 mmol) and In a 3000 L reactor, 201.6 kg of KOH was added, Pumped 253.2 kg of 3, 4, 5-trifluorobromobenzene and 1500 L of methanol, Close the reaction kettle, stirring up to 60 , After 6 hours of reaction, Raw materials have been basically complete.The material into the crystallization pot with nitrogen into the pot, Stirring and cooling to -5 ° C, Insulation 5h filter, To give 2, 3-difluoro-5-bromoanisole, Yield 92.0percentContent of 99.2percent. The methanol recovery in the filtrate can be reused.A mixture of A flask is charged with 5-Bromo-1, 2-difluoro-3-methoxy-benzene (400 mg, 1.79 mmol, 1 eq.), piperazine (927 mg, 10.76 mmol, 6 eq.), BINAP (134 mg, 0.215 mmol, 0.12 eq.), NaOtBu (241 mg, 2.511 mmol, 1.4 eq.) and toluene (3 mL). The reaction mixture is degassed with N2 and Pd2(dba)3 (99 mg, 0.108 mmol, 0.06 eq.) is added. Reaction mixture is heated at 100C overnight. The reaction mixture is extracted with HCl 1N solution. The aqueous layer is basified with NaOH 2N solution and extracted with DCM. The combined organic layers are washed with water and brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo to afford the expected product. LCMS: MW (calcd): 228. MW (obsd): 229 (M+H)A solution of 1-bromo-3, 4-difluoro-5-methoxy-benzene (1.11 g, 5.0 mmol, 1.0 eq.) and sodium methoxide (405 mg, 7.5 mmol, 1.5 eq.) in DMA (5 mL) is heated at 100C for 1h. The reaction mixture is then poured into 60 mL of water and ice, stirred and the resulting solid is filtered and dried under suction to afford the expected productA solution of 1-bromo-3, 4-difluoro-5-methoxy-benzene (1.11 g, 5.0 mmol, 1.0 eq.) and sodium methoxide (405 mg, 7.5 mmol, 1.5 eq.) in DMA (5 mL) is heated at 100C for lh. The reaction mixture is then poured into 60 ml. of water and ice, stirred and the resulting solid is filtered and dried under suction to afford the expected product.In a 50 mL round-bottom flask, introduce 1 g (4.48 mmol) of

Computed Properties

Molecular Weight:223.01
XLogP3:2.8
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:221.94918
Monoisotopic Mass:221.94918
Topological Polar Surface Area:9.2
Heavy Atom Count:11
Complexity:134
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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