C₁₇H₁₉BrO₉

Base Information

Chemical Name:C₁₇H₁₉BrO₉
CAS No.:1261975-05-6
Molecular Formula:C₁₇H₁₉BrO₉
Molecular Weight:447.236
Hs Code.:

C<sub>17</sub>H<sub>19</sub>BrO<sub>9</sub>

Synonyms:C₁₇H₁₉BrO₉

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Chemical Property of C₁₇H₁₉BrO₉

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Technology Process of C₁₇H₁₉BrO₉

There total 12 articles about C₁₇H₁₉BrO₉ 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:

: 1261974-88-2
C₁₇H₁₇BrO₇

: 1261975-05-6
C₁₇H₁₉BrO₉

Guidance literature:: C₁₇H₁₇BrO₇; With 4-methylmorpholine N-oxide; In water; acetone; at 20 ℃; for 0.0833333h;

With osmium(VIII) oxide; In water; acetone; at 20 ℃; for 14h;
DOI:10.1021/ol102848w

Reference yield:

: 1261974-82-6
(2S,3R,Z)-3-(dimethyl(phenyl)silyl)-5-ethoxy-1-methoxypent-4-en-2-ol

: 1261975-05-6
C₁₇H₁₉BrO₉

Guidance literature:: Multi-step reaction with 6 steps

1.1: toluene-4-sulfonic acid / dichloromethane / 0.17 h / 0 °C

2.1: phenyltrimethylammonium tribromide / tetrahydrofuran / 12 h / 20 °C

2.2: 0.17 h / 0 °C

3.1: sodium cyanide; manganese(IV) oxide / 4 h / 0 - 20 °C

4.1: 4-methylmorpholine N-oxide / water; acetone / 0.08 h / 20 °C

4.2: 10 h / 20 °C

5.1: dmap / dichloromethane / 0 - 20 °C / Inert atmosphere

6.1: 4-methylmorpholine N-oxide / water; acetone / 0.08 h / 20 °C

6.2: 14 h / 20 °C

With dmap; sodium cyanide; manganese(IV) oxide; phenyltrimethylammonium tribromide; toluene-4-sulfonic acid; 4-methylmorpholine N-oxide; In tetrahydrofuran; dichloromethane; water; acetone; 1.1: Mukaiyama reaction;
DOI:10.1021/ol102848w

Reference yield:

: 1261974-99-5
(2S,3R)-3-(dimethyl(phenyl)silyl)-5-ethoxy-1-methoxypent-4-yn-2-ol

: 1261975-05-6
C₁₇H₁₉BrO₉

Guidance literature:: Multi-step reaction with 7 steps

1.1: pyridine; Lindlar's catalyst; hydrogen / ethyl acetate / 1 h

2.1: toluene-4-sulfonic acid / dichloromethane / 0.17 h / 0 °C

3.1: phenyltrimethylammonium tribromide / tetrahydrofuran / 12 h / 20 °C

3.2: 0.17 h / 0 °C

4.1: sodium cyanide; manganese(IV) oxide / 4 h / 0 - 20 °C

5.1: 4-methylmorpholine N-oxide / water; acetone / 0.08 h / 20 °C

5.2: 10 h / 20 °C

6.1: dmap / dichloromethane / 0 - 20 °C / Inert atmosphere

7.1: 4-methylmorpholine N-oxide / water; acetone / 0.08 h / 20 °C

7.2: 14 h / 20 °C

With pyridine; dmap; sodium cyanide; manganese(IV) oxide; Lindlar's catalyst; hydrogen; phenyltrimethylammonium tribromide; toluene-4-sulfonic acid; 4-methylmorpholine N-oxide; In tetrahydrofuran; dichloromethane; water; ethyl acetate; acetone; 2.1: Mukaiyama reaction;
DOI:10.1021/ol102848w