Analyzing the synthesis route of 3663-79-4

With the synthetic route has been constantly updated, we look forward to future research findings about Methyl 1,4-Benzodioxane-2-carboxylate,belong benzodioxans compound

As a common heterocyclic compound, it belong benzodioxans compound,Methyl 1,4-Benzodioxane-2-carboxylate,3663-79-4,Molecular formula: C10H10O4,mainly used in chemical industry, its synthesis route is as follows.,3663-79-4

General procedure: Methyl 1,4-benzodioxan-2-carboxylate (¡À)-17a was dissolved in ? THF/ ? H2O (1:1 ratio) after which ? lithium hydroxide was added. The reaction was stirred for 3?h until hydrolysis was complete. Next, THF was evaporated and the residue acidified with 10percent HCl. DCM was used for extraction. The organic layers were dried in vacuo to give ? (¡À)-1,4-benzodioxan-2-carboxylic acid 1 in 91percent yield as a white solid; mp 117?119?¡ãC; [lit.23b 125.4]; 1H NMR: delta 4.44 (d, J?=?4.8?Hz, 2H), 4.90 (t, J?=?3.7, 7.6?Hz, 1H), 6.88?6.97 (m, 3H), 6.99?7.02 (m, 1H); 13C NMR: delta 64.63, 71.61, 117.34, 122.38, 141.97, 142.87 173.59; HRMS (ESI) Calcd for C9H8NaO4 (M+Na): 203.0320. Found: 203.0317.

With the synthetic route has been constantly updated, we look forward to future research findings about Methyl 1,4-Benzodioxane-2-carboxylate,belong benzodioxans compound

Reference£º
Article; Rouf, Abdul; Gupta, Pankaj; Aga, Mushtaq A.; Kumar, Brijesh; Chaubey, Asha; Parshad, Rajinder; Taneja, Subhash C.; Tetrahedron Asymmetry; vol. 23; 22-23; (2012); p. 1615 – 1623;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem

Analyzing the synthesis route of 3663-79-4

The synthetic route of 3663-79-4 has been constantly updated, and we look forward to future research findings.

3663-79-4, Methyl 1,4-Benzodioxane-2-carboxylate is a benzodioxans compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

General procedure: Methyl 1,4-benzodioxan-2-carboxylate (¡À)-17a was dissolved in ? THF/ ? H2O (1:1 ratio) after which ? lithium hydroxide was added. The reaction was stirred for 3?h until hydrolysis was complete. Next, THF was evaporated and the residue acidified with 10percent HCl. DCM was used for extraction. The organic layers were dried in vacuo to give ? (¡À)-1,4-benzodioxan-2-carboxylic acid 1 in 91percent yield as a white solid; mp 117?119?¡ãC; [lit.23b 125.4]; 1H NMR: delta 4.44 (d, J?=?4.8?Hz, 2H), 4.90 (t, J?=?3.7, 7.6?Hz, 1H), 6.88?6.97 (m, 3H), 6.99?7.02 (m, 1H); 13C NMR: delta 64.63, 71.61, 117.34, 122.38, 141.97, 142.87 173.59; HRMS (ESI) Calcd for C9H8NaO4 (M+Na): 203.0320. Found: 203.0317.

The synthetic route of 3663-79-4 has been constantly updated, and we look forward to future research findings.

Reference£º
Article; Rouf, Abdul; Gupta, Pankaj; Aga, Mushtaq A.; Kumar, Brijesh; Chaubey, Asha; Parshad, Rajinder; Taneja, Subhash C.; Tetrahedron Asymmetry; vol. 23; 22-23; (2012); p. 1615 – 1623;,
Benzodioxan
1,4-Benzodioxane | C8H8O2 – PubChem