C₁₇H₁₆O₃S₂

Base Information

Chemical Name:C₁₇H₁₆O₃S₂
CAS No.:1612882-25-3
Molecular Formula:C₁₇H₁₆O₃S₂
Molecular Weight:332.444
Hs Code.:

C<sub>17</sub>H<sub>16</sub>O<sub>3</sub>S<sub>2</sub>

Synonyms:

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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 C₁₇H₁₆O₃S₂

Chemical Property:

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Technology Process of C₁₇H₁₆O₃S₂

There total 4 articles about C₁₇H₁₆O₃S₂ 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:

: 1612882-15-1
C₁₇H₁₄O₃S₂

: C₁₇H₁₆O₃S₂

: 1612882-25-3
C₁₇H₁₆O₃S₂

Guidance literature:: With sodium tetrahydroborate; In methanol; at 0 ℃; for 0.5h;
DOI:10.1002/adsc.201300250

Reference yield:

: 1571-08-0
methyl 4-formylbenzoate

: 1612882-25-3
C₁₇H₁₆O₃S₂

Guidance literature:: Multi-step reaction with 4 steps

1: lithium hexamethyldisilazane / tetrahydrofuran / 20 h / 0 °C

2: hydrogenchloride / tetrahydrofuran; water / Reflux

3: (5S)-(?)-2,2,3-trimethyl-5-benzyl-4-imidazolidinone monohydrochloride / water; acetonitrile / 24 h / 0 °C

4: sodium tetrahydroborate / methanol / 0.5 h / 0 °C

With hydrogenchloride; sodium tetrahydroborate; lithium hexamethyldisilazane; (5S)-(?)-2,2,3-trimethyl-5-benzyl-4-imidazolidinone monohydrochloride; In tetrahydrofuran; methanol; water; acetonitrile;
DOI:10.1002/adsc.201300250

Reference yield:

: 119770-38-6
cis-1-methoxy-2-(4-carbomethoxyphenyl)ethylene

: 1612882-25-3
C₁₇H₁₆O₃S₂

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride / tetrahydrofuran; water / Reflux

2: (5S)-(?)-2,2,3-trimethyl-5-benzyl-4-imidazolidinone monohydrochloride / water; acetonitrile / 24 h / 0 °C

3: sodium tetrahydroborate / methanol / 0.5 h / 0 °C

With hydrogenchloride; sodium tetrahydroborate; (5S)-(?)-2,2,3-trimethyl-5-benzyl-4-imidazolidinone monohydrochloride; In tetrahydrofuran; methanol; water; acetonitrile;
DOI:10.1002/adsc.201300250