Methyl 4-chloro-3-methoxy-5-nitrobenzenecarboxylate

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Methyl 4-chloro-3-methoxy-5-nitrobenzenecarboxylate Basic information
Product Name:Methyl 4-chloro-3-methoxy-5-nitrobenzenecarboxylate
Synonyms:Methyl 4-chloro-3-methoxy-5-nitrobenzenecarboxylate;Methyl 4-chloro-3-methoxy-5-nitrobenzoate 95+%;2-Chloro-5-(methoxycarbonyl)-3-nitroanisole;2-Chloro-5-(methoxycarbonyl)-3-nitroanisole, Methyl 4-chloro-5-nitro-m-anisate;methyl 3-nitro-4-chloro-5-methoxybenzoate;2-chloro-1-methoxy-5-(methylperoxy)-3-nitrobenzene;Benzoic acid, 4-chloro-3-methoxy-5-nitro-, methyl ester;Benzeneaceticacid,6-bromo-α-formyl-,ethylester
CAS:63603-09-8
MF:C9H8ClNO5
MW:245.62
EINECS:
Product Categories:
Mol File:63603-09-8.mol
Methyl 4-chloro-3-methoxy-5-nitrobenzenecarboxylate Structure
Methyl 4-chloro-3-methoxy-5-nitrobenzenecarboxylate Chemical Properties
Boiling point 366.2±37.0 °C(Predicted)
density 1.402±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form crystalline powder
color Beige to light brown
InChIInChI=1S/C9H8ClNO5/c1-15-7-4-5(9(12)16-2)3-6(8(7)10)11(13)14/h3-4H,1-2H3
InChIKeyQNYHMMOXMRPWTK-UHFFFAOYSA-N
SMILESC(OC)(=O)C1=CC([N+]([O-])=O)=C(Cl)C(OC)=C1
Safety Information
HazardClass IRRITANT
HS Code 2922500090
MSDS Information
Methyl 4-chloro-3-methoxy-5-nitrobenzenecarboxylate Usage And Synthesis
UsesMethyl 4-Chloro-3-methoxy-5-nitrobenzoate is a reagent in the formal total synthesis of N-methylmaysenine.
Synthesis
Methyl 4-hydroxy-3-methoxy-5-nitrobenzenecarboxylate

42590-00-1

Methyl 4-chloro-3-methoxy-5-nitrobenzenecarboxylate

63603-09-8

Step (ii): synthesis of methyl 4-chloro-3-methoxy-5-nitrobenzoate (3) Methyl 4-hydroxy-3-methoxy-5-nitrobenzoate (2) (4.4 g, 19 mmol) was dissolved in DMF (30 mL) at 0 °C and oxalyl chloride (5.09 mL, 58.1 mmol) was added dropwise. The reaction mixture was stirred at 80 °C for 3 h under the protection of a CaCl2 drying tube. After completion of the reaction, the mixture was cooled to room temperature, slowly poured into ice water (100 mL) and stirred for 15 minutes. The precipitate was collected by filtration and washed sequentially with water and methanol to afford methyl 4-chloro-3-methoxy-5-nitrobenzoate (3) as a yellow solid (3.2 g, 65% yield). The product was characterized by 1H NMR (400 MHz, CDCl3): δ 8.04 (1H, d), 7.77 (1H, d), 4.04 (3H, s), 3.97 (3H, s).

References[1] Organic Letters, 2009, vol. 11, # 8, p. 1809 - 1812
[2] Journal of the American Chemical Society, 1983, vol. 105, # 15, p. 5015 - 5024
[3] Patent: WO2011/27106, 2011, A1. Location in patent: Page/Page column 152
[4] Patent: US2012/149737, 2012, A1. Location in patent: Page/Page column 89
Methyl 4-chloro-3-methoxy-5-nitrobenzenecarboxylate Preparation Products And Raw materials
Raw materialsMethyl 4-hydroxy-3-methoxy-5-nitrobenzenecarboxylate-->Methyl vanillate
Preparation Products4-Chloro-3-nitrobenzamide-->Methyl 4-chloro-3-hydroxy-5-nitrobenzoate
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