CAS No.29662-90-6,2,2-Dimethyloctanoic acid Suppliers

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2,2-Dimethyloctanoic acid CAS：29662-90-6

Cas:29662-90-6

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2,2-Dimethyloctanoic acid

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2,2-Dimethyloctanoic acid

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Shandong Mopai Biotechnology Co., LTD

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2,2-Dimethyloctanoic acid

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Henan Tianfu Chemical Co., Ltd.

2,2-Dimethyloctanoic acid Application:Organic Chemicals

2,2-Dimethyloctanoic acid

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Antimex Chemical Limied

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Hangzhou Sartort Biopharma Co., Ltd

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2,2-Dimethyloctanoicacid

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ZHEJIANG JIUZHOU CHEM CO.,LTD

factory?direct?saleAppearance:White powder Storage:Sealed and preserved Package:200/Kilograms Application:healing drugs Transportation:By sea Port:Shanghai/tianjin

2,2-Dimethyloctanoic acid

Cas:29662-90-6

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Synthetic route

: 638-45-9
1-Iodohexane

: 79-31-2
isobutyric Acid

: 29662-90-6
dimethyloctanoic acid

Conditions

Conditions	Yield
Stage #1: isobutyric Acid With hydrogenchloride; lithium diisopropyl amide In ethanol at 0℃; for 0.25h; Inert atmosphere; Stage #2: 1-Iodohexane at 0 - 20℃; for 2h;	63.4%
Stage #1: isobutyric Acid With lithium diisopropyl amide In tetrahydrofuran at -78 - 20℃; for 1h; Stage #2: 1-Iodohexane In tetrahydrofuran at -78 - 20℃;
Stage #1: isobutyric Acid With lithium diisopropyl amide In tetrahydrofuran at -78 - 20℃; Stage #2: 1-Iodohexane In tetrahydrofuran at -78 - 20℃;

: 103906-30-5
2,2-dimethyloctanamide

: 29662-90-6
dimethyloctanoic acid

Conditions

Conditions	Yield
With 1,4-dioxane; hydrogenchloride; n-Butyl nitrite
With sulfuric acid; sodium nitrite
With nitro, sulfate; sulfuric acid; water at 45 - 60℃;

: 124-11-8
non-1-ene

: 201230-82-2
carbon monoxide

A: 31080-38-3
2-methyl-2-ethyl heptanoic acid

B: 29662-90-6
dimethyloctanoic acid

C: 31080-37-2
2-methyl-2-propylhexanoic acid

Conditions

Conditions	Yield
(i) BF3*H2SO4, (ii) H2O; Multistep reaction;

...Expand

: 592-41-6
1-hexene

: 79-31-2
isobutyric Acid

: 29662-90-6
dimethyloctanoic acid

Conditions

Conditions	Yield
With di-tert-butyl peroxide

: 64-18-6
formic acid

: 628-44-4
2-methyl-2-octanol

: 29662-90-6
dimethyloctanoic acid

Conditions

Conditions	Yield
With sulfuric acid 1.) carbon tetrachloride, 5 deg C, 3 min, 2.) 5 deg C, 4.5 h; Yield given. Multistep reaction;

: 124-11-8
non-1-ene

: 201230-82-2
carbon monoxide

A: 31080-38-3
2-methyl-2-ethyl heptanoic acid

B: 29662-90-6
dimethyloctanoic acid

C: 25234-25-7
nonane-3-carboxylic acid

D: 31080-37-2
2-methyl-2-propylhexanoic acid

Conditions

Conditions	Yield
With copper(I) oxide; (BF3H2O)(BF3H3PO4) at 30℃; under 760 Torr; for 4h; Product distribution; other catalyst;	A 50 % Turnov. B 26 % Turnov. C 15 % Turnov. D 9 % Turnov.

...Expand

: 74-85-1
ethene

: 79-31-2
isobutyric Acid

A: 29662-90-6
dimethyloctanoic acid

B other carboxylic acids: other carboxylic acids

Conditions

Conditions	Yield
With oxygen; 1,2-di(benzylidene)hydrazine at 275℃; under 514855 Torr;

...Expand

: 873416-40-1
2,2-dimethyl-1-phenyl-octan-1-one

: 29662-90-6
dimethyloctanoic acid

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: NaNH2; benzene 2: concentrated H2SO4; NaNO2 View Scheme
Multi-step reaction with 2 steps 1: NaNH2; toluene 2: concentrated H2SO4; (NO2)2SO4; water / 45 - 60 °C View Scheme

: 2,2-dimethyl-3-octenoic acid

: 29662-90-6
dimethyloctanoic acid

Conditions

Conditions	Yield
With N2; palladium In ethanol

: 111-25-1
1-bromo-hexane

: 79-31-2
isobutyric Acid

: 29662-90-6
dimethyloctanoic acid

Conditions

Conditions	Yield
With n-butyllithium; nitrogen; diisopropylamine In tetrahydrofuran; diethyl ether; hexane; water; mineral oil

: 59415-01-9
ethyl 2,2-dimethyloctanoate

: 29662-90-6
dimethyloctanoic acid

Conditions

Conditions	Yield
With sodium hydroxide In methanol; water for 2h; Reflux;

: 638-45-9
1-Iodohexane

: 29662-90-6
dimethyloctanoic acid

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1.1: lithium diisopropyl amide / tetrahydrofuran / 1 h / -78 °C 1.2: -78 - 20 °C 2.1: sodium hydroxide / water; methanol / 2 h / Reflux View Scheme

: 29662-90-6
dimethyloctanoic acid

: neodymium(III) chloride hydrate

: neodymium neodecanoate

Conditions

Conditions	Yield
Stage #1: dimethyloctanoic acid With sodium hydroxide In ethanol; water at 20℃; for 1h; Stage #2: neodymium(III) chloride hydrate In ethanol; hexane; water at 20℃; for 15h;	96%

: 29662-90-6
dimethyloctanoic acid

: 103-16-2
4-Benzyloxyphenol

: 4-(benzyloxy)phenyl 2,2-dimethyloctanoate

Conditions

Conditions	Yield
Stage #1: dimethyloctanoic acid With oxalyl dichloride; triethylamine In dichloromethane at 0℃; for 2h; Inert atmosphere; Stage #2: 4-Benzyloxyphenol With triethylamine; N,N-dimethyl-formamide In dichloromethane at 0 - 20℃; for 15h;	49%

: 29662-90-6
dimethyloctanoic acid

: 17701-32-5
2,2-dimethyloctanoic acid chloride

Conditions

Conditions	Yield
With thionyl chloride
With thionyl chloride for 1h; Reflux;
With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃;
With thionyl chloride In benzene for 4h; Reflux;

: 29662-90-6
dimethyloctanoic acid

sodium-salt of/the/ 2,2-dimethyl-octanoic acid: sodium-salt of/the/ 2,2-dimethyl-octanoic acid

A: 111-66-0
oct-1-ene

B: 4588-18-5
2-methyl-1-octene

C 2-methyl-oct-2-ene(?): 2-methyl-oct-2-ene(?)

Conditions

Conditions	Yield
at 400℃;

...Expand

: 29662-90-6
dimethyloctanoic acid

: 103906-30-5
2,2-dimethyloctanamide

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: thionyl chloride 2: water; ammonia View Scheme

: 29662-90-6
dimethyloctanoic acid

: 97725-04-7
2,2-dimethyl-octanoic acid anilide

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: thionyl chloride View Scheme

: 29662-90-6
dimethyloctanoic acid

A: 5-benzoyl-4-butyl-2,2-dimethylcyclopentanone

B: 4-benzoyl-2,2-dimethyl-3-pentylcyclobutanone

Conditions

Conditions	Yield
Multi-step reaction with 6 steps 1: thionyl chloride / 1 h / Reflux 2: pyridine / dichloromethane / 0 - 20 °C 3: tetrahydrofuran / -78 - 20 °C 4: C7H16AuO3S; water / methanol / 12 h / 70 °C 5: triethylamine; 4-toluenesulfonyl azide / acetonitrile / 4 h / 0 - 20 °C 6: t-BuBrettPhosAuNTf2; 8-isopropyl-quinoline-N-oxide / 1,2-dichloro-ethane / 96 h / 20 °C View Scheme

: 29662-90-6
dimethyloctanoic acid

: 4-butyl-2,2-dimethyl-5-pentanoylcyclopentanone

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: thionyl chloride / 1 h / Reflux 2: pyridine / dichloromethane / 0 - 20 °C 3: tetrahydrofuran / -78 - 20 °C 4: C33H48NPAu(1+)Cl(1-); silver(I) triflimide; 8-isopropyl-quinoline-N-oxide / fluorobenzene / 2 h / 20 °C View Scheme

: 29662-90-6
dimethyloctanoic acid

: 4-benzoyl-2,2-dimethyl-3-pentylcyclobutanone

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: thionyl chloride / 1 h / Reflux 2: pyridine / dichloromethane / 0 - 20 °C 3: tetrahydrofuran / -78 - 20 °C 4: t-BuBrettPhosAuNTf2; 8-isopropyl-quinoline-N-oxide / 1,2-dichloro-ethane / 2 h / 20 °C View Scheme
Multi-step reaction with 4 steps 1: thionyl chloride / 1 h / Reflux 2: pyridine / dichloromethane / 0 - 20 °C 3: tetrahydrofuran / -78 - 20 °C 4: 8-methylquinoline 1-oxide; C33H48NPAu(1+)Cl(1-) / fluorobenzene / 12 h / 20 °C View Scheme
Multi-step reaction with 4 steps 1: thionyl chloride / 1 h / Reflux 2: pyridine / dichloromethane / 0 - 20 °C 3: tetrahydrofuran / -78 - 20 °C 4: 8-methylquinoline 1-oxide; silver(I) triflimide; (1,3-dimesitylimidazol-2-ylidene)gold(I) chloride / fluorobenzene / 2 h / 20 °C View Scheme
Multi-step reaction with 4 steps 1: thionyl chloride / 1 h / Reflux 2: pyridine / dichloromethane / 0 - 20 °C 3: tetrahydrofuran / -78 - 20 °C 4: 8-methylquinoline 1-oxide; C33H48NPAu(1+)Cl(1-); silver(I) triflimide / fluorobenzene / 2 h / 20 °C View Scheme

: 29662-90-6
dimethyloctanoic acid

: 4,4-dimethyl-1-phenyldec-1-yn-3-one

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: thionyl chloride / 1 h / Reflux 2: pyridine / dichloromethane / 0 - 20 °C 3: tetrahydrofuran / -78 - 20 °C View Scheme

: 29662-90-6
dimethyloctanoic acid

: 8,8-dimethyltetradec-5-yn-7-one

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: thionyl chloride / 1 h / Reflux 2: pyridine / dichloromethane / 0 - 20 °C 3: tetrahydrofuran / -78 - 20 °C View Scheme

: 29662-90-6
dimethyloctanoic acid

: N-methoxy-N,2,2-trimethyloctanamide

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: thionyl chloride / 1 h / Reflux 2: pyridine / dichloromethane / 0 - 20 °C View Scheme
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide; oxalyl dichloride / dichloromethane / 20 °C 2: dmap; pyridine / dichloromethane / 0 - 20 °C View Scheme

: 29662-90-6
dimethyloctanoic acid

: 2-diazo-4,4-dimethyl-1-phenyldecane-1,3-dione

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1: thionyl chloride / 1 h / Reflux 2: pyridine / dichloromethane / 0 - 20 °C 3: tetrahydrofuran / -78 - 20 °C 4: C7H16AuO3S; water / methanol / 12 h / 70 °C 5: triethylamine; 4-toluenesulfonyl azide / acetonitrile / 4 h / 0 - 20 °C View Scheme

: 29662-90-6
dimethyloctanoic acid

: C18H26O2

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: thionyl chloride / 1 h / Reflux 2: pyridine / dichloromethane / 0 - 20 °C 3: tetrahydrofuran / -78 - 20 °C 4: C7H16AuO3S; water / methanol / 12 h / 70 °C View Scheme

: 29662-90-6
dimethyloctanoic acid

: 858491-52-8
1,1-dimethyl-heptyl isocyanate

Conditions

Conditions	Yield
With diphenylphosphoranyl azide; triethylamine In toluene at 0 - 100℃; for 14h; Inert atmosphere;

: 29662-90-6
dimethyloctanoic acid

: 1,1-dimethylheptylamine hydrochloride

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: diphenylphosphoranyl azide; triethylamine / toluene / 14 h / 0 - 100 °C / Inert atmosphere 2: hydrogenchloride / water; acetic acid / 20 °C View Scheme

: 29662-90-6
dimethyloctanoic acid

: 2626-63-3
1,1-dimethylheptylamine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: diphenylphosphoranyl azide; triethylamine / toluene / 14 h / 0 - 100 °C / Inert atmosphere 2: hydrogenchloride / water; acetic acid / 20 °C View Scheme

: 29662-90-6
dimethyloctanoic acid

: C17H38AlN

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: diphenylphosphoranyl azide; triethylamine / toluene / 14 h / 0 - 100 °C / Inert atmosphere 2: hydrogenchloride / water; acetic acid / 20 °C 3: tetrahydrofuran; toluene / 2 h / 0 - 20 °C / Inert atmosphere View Scheme

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