C₁₇H₁₆O₂

Base Information

Chemical Name:C₁₇H₁₆O₂
CAS No.:1478662-27-9
Molecular Formula:C₁₇H₁₆O₂
Molecular Weight:252.313
Hs Code.:

C<sub>17</sub>H<sub>16</sub>O<sub>2</sub>

Synonyms:C₁₇H₁₆O₂

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Chemical Property of C₁₇H₁₆O₂

Chemical Property:

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Technology Process of C₁₇H₁₆O₂

There total 12 articles about C₁₇H₁₆O₂ 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:

: C₁₉H₁₈O₃

: 1478662-27-9
C₁₇H₁₆O₂

Guidance literature:: With hydrogenchloride; In tetrahydrofuran; water; at 0 - 20 ℃; for 24h;
DOI:10.1055/s-0033-1339484

Reference yield:

: C₂₄H₃₄O₂Si

: 1478662-27-9
C₁₇H₁₆O₂

Guidance literature:: Multi-step reaction with 7 steps

1: Dess-Martin periodane; sodium hydrogencarbonate / dichloromethane / 3 h / 0 - 20 °C

2: tetrahydrofuran / 1 h / 0 - 20 °C

3: Dess-Martin periodane; sodium hydrogencarbonate / dichloromethane / 0.5 h / 0 - 20 °C

4: tetrabutyl ammonium fluoride / tetrahydrofuran / 12 h / 0 - 20 °C

5: 3-chloro-benzenecarboperoxoic acid; scandium tris(trifluoromethanesulfonate) / dichloromethane / 72 h / 0 - 20 °C / Inert atmosphere

6: Dess-Martin periodane; sodium hydrogencarbonate / dichloromethane / 2.5 h / 0 - 20 °C

7: hydrogenchloride / tetrahydrofuran; water / 24 h / 0 - 20 °C

With hydrogenchloride; tetrabutyl ammonium fluoride; sodium hydrogencarbonate; Dess-Martin periodane; 3-chloro-benzenecarboperoxoic acid; scandium tris(trifluoromethanesulfonate); In tetrahydrofuran; dichloromethane; water; 5: |Baeyer-Villiger Ketone Oxidation;
DOI:10.1055/s-0033-1339484

Reference yield:

: 1477494-13-5
ethyl 4-[7-(tert-butyldimethylsilanyloxymethyl)-1-methylindan-4-yl]benzoate

: 1478662-27-9
C₁₇H₁₆O₂

Guidance literature:: Multi-step reaction with 8 steps

1: lithium borohydride / tetrahydrofuran / 20 h / 0 - 50 °C / Inert atmosphere

2: Dess-Martin periodane; sodium hydrogencarbonate / dichloromethane / 3 h / 0 - 20 °C

3: tetrahydrofuran / 1 h / 0 - 20 °C

4: Dess-Martin periodane; sodium hydrogencarbonate / dichloromethane / 0.5 h / 0 - 20 °C

5: tetrabutyl ammonium fluoride / tetrahydrofuran / 12 h / 0 - 20 °C

6: 3-chloro-benzenecarboperoxoic acid; scandium tris(trifluoromethanesulfonate) / dichloromethane / 72 h / 0 - 20 °C / Inert atmosphere

7: Dess-Martin periodane; sodium hydrogencarbonate / dichloromethane / 2.5 h / 0 - 20 °C

8: hydrogenchloride / tetrahydrofuran; water / 24 h / 0 - 20 °C

With hydrogenchloride; lithium borohydride; tetrabutyl ammonium fluoride; sodium hydrogencarbonate; Dess-Martin periodane; 3-chloro-benzenecarboperoxoic acid; scandium tris(trifluoromethanesulfonate); In tetrahydrofuran; dichloromethane; water; 6: |Baeyer-Villiger Ketone Oxidation;
DOI:10.1055/s-0033-1339484