| Identification | Back Directory | [Name]
(S)-3-METHYLHEPTANOIC ACID | [CAS]
59614-85-6 | [Synonyms]
(S)-3-METHYLHEPTANOIC ACID
Heptanoic acid,3-methyl-, (3S)- | [Molecular Formula]
C8H16O2 | [MDL Number]
MFCD04112705 | [MOL File]
59614-85-6.mol | [Molecular Weight]
144.21 |
| Chemical Properties | Back Directory | [Boiling point ]
234.6℃ | [density ]
0.926 | [Fp ]
116.6℃ | [pka]
4.80±0.10(Predicted) | [InChI]
InChI=1S/C8H16O2/c1-3-4-5-7(2)6-8(9)10/h7H,3-6H2,1-2H3,(H,9,10)/t7-/m0/s1 | [InChIKey]
DVESMWJFKVAFSP-ZETCQYMHSA-N | [SMILES]
C(O)(=O)C[C@@H](C)CCCC |
| Hazard Information | Back Directory | [Uses]
(S)-3-Methylheptanoic acid is a chiral organic acid compound that can be used as a synthetic unit in the synthesis of PGI2 (prostacyclin I2) analogues, such as pimiprost and ronoprost[1]. | [Synthesis]
The synthesis of (S)-3-methylheptanoic acid begins with a chemically selective alkylation reaction between bromo-propylmagnesium and bromoester 3 under Cu(I) catalysis, yielding ester 6 in very high yield. Subsequently, a Barbier–Villain dealkylation reaction was employed to remove an excess carbon atom from 6. Ester 6 reacts with phenylmagnesium bromide to form alcohol 7, which undergoes efficient dehydration in DCM in the presence of a catalytic amount of TMSCl to yield the diphenyl alkene 8. Oxidation of 8 with KMnO₄/NaIO₄ in a t-butanol–water system cleaves the double bond, yielding the target product 1 in 84% yield. Oxidation of 8 with ozone in ethyl acetate, followed by treatment of the resulting mixture with 30% hydrogen peroxide/1.2 mol·L⁻¹ hydrochloric acid, similarly yielded 1 in higher yield. Optically pure compound 1 (91.0% ee) was obtained via its derivative 9.[1]
 | [References]
[1] Shunji Zhang, Weisheng T., Yong Shi. (2015). Syntheses of (R)- and (S)-3-Methylheptanoic Acids. Chinese Journal of Chemistry, 33 6, 674–678. https://doi.org/10.1002/cjoc.201400861 |
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| Company Name: |
Tetranov Biopharm
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| Tel: |
13526569071 |
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http://www.leadmedpharm.com/index.html |
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