(S)-1,4-Benzodioxane-2-carboxylic acid
(S)-1,4-Benzodioxane-2-carboxylic acid Basic information
- Product Name:
- (S)-1,4-Benzodioxane-2-carboxylic acid
- Synonyms:
-
- (2S)-2,3-dihydro-1,4-benzodioxine-2-carboxylic acid
- (S)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-CARBOXYLIC ACID
- (S)-1,4-BENZODIOXANE-2-CARBOXYLIC ACID
- (S)-1,4-BENZODIOXAN 2-CARBOXYLIC ACID
- (S)-2,3-DIHYDRO-BENZO[1,4]DIOXINE-2-CARBOXYLIC ACID
- (S)-2,3-dihydrobenzo[b][1,4]dioxine-2-carboxylic acid
- Afalanine [INN]
- (3S)-2,3-Dihydro-1,4-benzodioxine-3-carboxylic acid
- CAS:
- 70918-54-6
- MF:
- C9H8O4
- MW:
- 180.16
- Mol File:
- 70918-54-6.mol
(S)-1,4-Benzodioxane-2-carboxylic acid Chemical Properties
- Melting point:
- 96-99 °C
- Boiling point:
- 347.2±41.0 °C(Predicted)
- alpha
- -83 º (c=1.5% in chloroform)
- Density
- 1.379±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 2.69±0.20(Predicted)
- Appearance
- White to off-white Solid
- optical activity
- [α]20/D 83±2°, c = 1.5% in chloroform
- BRN
- 5742836
MSDS
- Language:English Provider:SigmaAldrich
(S)-1,4-Benzodioxane-2-carboxylic acid Usage And Synthesis
Chemical Properties
White crystalline powder
Uses
(S)-2,3-Dihydrobenzo[1,4]dioxine-2-carboxylic Acid is an intermediate used to prepare 2-[4-(1,4-Benzodioxan-2-ylcarbonyl)piperazin-1-yl] derivatives as α1-adrenoceptor antagonists and antihypertensive agents. It is also used to synthesize G protein-coupled receptor antagonists.
Synthesis
3663-82-9
3663-80-7
1. Weigh (2,3-dihydrobenzo[b][1,4]dioxohexen-2-yl)methanol (compound b) and dissolve in 0.3 N aqueous KOH (1.3 equiv). 2. KMnO4 (2.0 eq.) was slowly added at 0 °C. 3. The reaction mixture was stirred at low temperature for about 10 minutes, followed by stirring at room temperature overnight. 4. After completion of the reaction, the organic phase was extracted with dichloromethane. 5. The organic phase was washed with water and subsequently dried with anhydrous sodium sulfate and concentrated to give a white solid, the crude product of 4-benzodioxane-2-carboxylic acid (compound c). 6. The crude product was purified by rapid chromatography on silica gel in 92.5% yield.
References
[1] Patent: CN105985328, 2016, A. Location in patent: Paragraph 0063; 0071; 0072
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