(+/-)-2-hydroxymethyl-2,6-dimethyl-1-cyclohexanone

Base Information

Chemical Name:(+/-)-2-hydroxymethyl-2,6-dimethyl-1-cyclohexanone
CAS No.:13756-98-4
Molecular Formula:C₉H₁₆O₂
Molecular Weight:156.225
Hs Code.:

Synonyms:(+/-)-2-hydroxymethyl-2,6-dimethyl-1-cyclohexanone

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (+/-)-2-hydroxymethyl-2,6-dimethyl-1-cyclohexanone

Chemical Property:

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Technology Process of (+/-)-2-hydroxymethyl-2,6-dimethyl-1-cyclohexanone

There total 9 articles about (+/-)-2-hydroxymethyl-2,6-dimethyl-1-cyclohexanone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 87787-09-5
6-hydroxymethyl-6-methyl-1,4-dioxaspiro<4.5>decane

: 13756-98-4
(+/-)-2-hydroxymethyl-2,6-dimethyl-1-cyclohexanone

Guidance literature:: Multi-step reaction with 6 steps

1: 7.43 g / di-isopropylethylamine / CH₂Cl₂ / Ambient temperature

2: pyridinium toluene-p-sulphonate / acetone / Heating

3: 90 percent / NaH / tetrahydrofuran / 3 h / Heating

4: NaH / 1.) THF, 0 deg C, 30 min, 2. a) 0 deg C, 40 min, b) RT

5: 40 percent / LiCl / hexamethylphosphoric acid triamide / 2 h / 120 °C

6: conc. H₂SO₄ / ethanol / 3 h / Heating

With sulfuric acid; pyridinium p-toluenesulfonate; sodium hydride; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; ethanol; dichloromethane; acetone;
DOI:10.1039/P19900001901

Reference yield:

: 13839-77-5
Ethyl 6-methyl-1,4-dioxaspiro[4.5]decane-6-carboxylate

: 13756-98-4
(+/-)-2-hydroxymethyl-2,6-dimethyl-1-cyclohexanone

Guidance literature:: Multi-step reaction with 7 steps

1: LiAlH₄ / diethyl ether / 0.5 h / Ambient temperature

2: 7.43 g / di-isopropylethylamine / CH₂Cl₂ / Ambient temperature

3: pyridinium toluene-p-sulphonate / acetone / Heating

4: 90 percent / NaH / tetrahydrofuran / 3 h / Heating

5: NaH / 1.) THF, 0 deg C, 30 min, 2. a) 0 deg C, 40 min, b) RT

6: 40 percent / LiCl / hexamethylphosphoric acid triamide / 2 h / 120 °C

7: conc. H₂SO₄ / ethanol / 3 h / Heating

With lithium aluminium tetrahydride; sulfuric acid; pyridinium p-toluenesulfonate; sodium hydride; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; ethanol; dichloromethane; acetone;
DOI:10.1039/P19900001901

Reference yield:

: 66088-37-7,5453-94-1
ethyl 1-methyl-2-oxocyclohexancarboxylate

: 13756-98-4
(+/-)-2-hydroxymethyl-2,6-dimethyl-1-cyclohexanone

Guidance literature:: Multi-step reaction with 8 steps

1: 96 percent / toluene-p-sulphonic acid monohydrate / benzene / Heating

2: LiAlH₄ / diethyl ether / 0.5 h / Ambient temperature

3: 7.43 g / di-isopropylethylamine / CH₂Cl₂ / Ambient temperature

4: pyridinium toluene-p-sulphonate / acetone / Heating

5: 90 percent / NaH / tetrahydrofuran / 3 h / Heating

6: NaH / 1.) THF, 0 deg C, 30 min, 2. a) 0 deg C, 40 min, b) RT

7: 40 percent / LiCl / hexamethylphosphoric acid triamide / 2 h / 120 °C

8: conc. H₂SO₄ / ethanol / 3 h / Heating

With lithium aluminium tetrahydride; sulfuric acid; pyridinium p-toluenesulfonate; sodium hydride; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; lithium chloride; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; ethanol; dichloromethane; acetone; benzene;
DOI:10.1039/P19900001901