7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-oxo-hept-2-enoic acid methyl ester

Base Information

Chemical Name:7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-oxo-hept-2-enoic acid methyl ester
CAS No.:288591-02-6
Molecular Formula:C₂₀H₃₀O₄Si
Molecular Weight:362.541
Hs Code.:

7-[3-(<i>tert</i>-butyl-dimethyl-silanyloxy)-phenyl]-7-oxo-hept-2-enoic acid methyl ester

Synonyms:7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-oxo-hept-2-enoic acid methyl ester

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Chemical Property of 7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-oxo-hept-2-enoic acid methyl ester

Chemical Property:

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Technology Process of 7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-oxo-hept-2-enoic acid methyl ester

There total 7 articles about 7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-oxo-hept-2-enoic acid methyl ester 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:

: 2398-37-0
3-methoxyphenyl bromide

: 288591-02-6
7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-oxo-hept-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: Mg / tetrahydrofuran / 20 °C

2: aq. HCl

3: 100 percent / pyridinium hydrochloride / 150 °C

4: 94 percent / Et₃N; DMAP / CH₂Cl₂ / 0 - 20 °C

5: 72 percent / N-methylmorpholine oxide; OsO₄ / acetone; H₂O / 20 °C

6: 97 percent / sodium metaperiodate / tetrahydrofuran; H₂O / 20 °C

7: tetrahydrofuran / 20 °C

With hydrogenchloride; dmap; sodium periodate; osmium(VIII) oxide; pyridine hydrochloride; magnesium; 4-methylmorpholine N-oxide; triethylamine; In tetrahydrofuran; dichloromethane; water; acetone; 1: Grignard reaction / 2: Dehydration / 3: Demethylation / 4: Silylation / 5: Dihydroxylation / 6: Oxidation / 7: Condensation;
DOI:10.1016/S0960-894X(00)00230-4

Reference yield:

: 36742-36-6
1-(3-methoxyphenyl)cyclopentene

: 288591-02-6
7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-oxo-hept-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 100 percent / pyridinium hydrochloride / 150 °C

2: 94 percent / Et₃N; DMAP / CH₂Cl₂ / 0 - 20 °C

3: 72 percent / N-methylmorpholine oxide; OsO₄ / acetone; H₂O / 20 °C

4: 97 percent / sodium metaperiodate / tetrahydrofuran; H₂O / 20 °C

5: tetrahydrofuran / 20 °C

With dmap; sodium periodate; osmium(VIII) oxide; pyridine hydrochloride; 4-methylmorpholine N-oxide; triethylamine; In tetrahydrofuran; dichloromethane; water; acetone; 1: Demethylation / 2: Silylation / 3: Dihydroxylation / 4: Oxidation / 5: Condensation;
DOI:10.1016/S0960-894X(00)00230-4

Reference yield:

: 120-92-3
cyclopentanone

: 288591-02-6
7-[3-(tert-butyl-dimethyl-silanyloxy)-phenyl]-7-oxo-hept-2-enoic acid methyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: Mg / tetrahydrofuran / 20 °C

2: aq. HCl

3: 100 percent / pyridinium hydrochloride / 150 °C

4: 94 percent / Et₃N; DMAP / CH₂Cl₂ / 0 - 20 °C

5: 72 percent / N-methylmorpholine oxide; OsO₄ / acetone; H₂O / 20 °C

6: 97 percent / sodium metaperiodate / tetrahydrofuran; H₂O / 20 °C

7: tetrahydrofuran / 20 °C

With hydrogenchloride; dmap; sodium periodate; osmium(VIII) oxide; pyridine hydrochloride; magnesium; 4-methylmorpholine N-oxide; triethylamine; In tetrahydrofuran; dichloromethane; water; acetone; 1: Grignard reaction / 2: Dehydration / 3: Demethylation / 4: Silylation / 5: Dihydroxylation / 6: Oxidation / 7: Condensation;
DOI:10.1016/S0960-894X(00)00230-4