Benzoic acid (1S,3S)-3-hydroxy-1,3-dihydro-isobenzofuran-1-ylmethyl ester

Base Information

Chemical Name:Benzoic acid (1S,3S)-3-hydroxy-1,3-dihydro-isobenzofuran-1-ylmethyl ester
CAS No.:528584-56-7
Molecular Formula:C₁₆H₁₄O₄
Molecular Weight:270.285
Hs Code.:

Synonyms:Benzoic acid (1S,3S)-3-hydroxy-1,3-dihydro-isobenzofuran-1-ylmethyl ester

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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 Benzoic acid (1S,3S)-3-hydroxy-1,3-dihydro-isobenzofuran-1-ylmethyl ester

Chemical Property:

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Technology Process of Benzoic acid (1S,3S)-3-hydroxy-1,3-dihydro-isobenzofuran-1-ylmethyl ester

There total 11 articles about Benzoic acid (1S,3S)-3-hydroxy-1,3-dihydro-isobenzofuran-1-ylmethyl 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: 90.0%

: 320600-36-0
(S)-1-O-Benzoyl-2-[2-(1,3-dioxan-2-yl)phenyl]ethane-1,2-diol

: 528584-56-7
Benzoic acid (1S,3S)-3-hydroxy-1,3-dihydro-isobenzofuran-1-ylmethyl ester

Guidance literature:: With toluene-4-sulfonic acid; In water; acetone; for 2.5h; Heating;
DOI:10.1039/b006417n

Reference yield:

: 643-79-8
o-phthalic dicarboxaldehyde

: 528584-56-7
Benzoic acid (1S,3S)-3-hydroxy-1,3-dihydro-isobenzofuran-1-ylmethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 50 percent / PTSA / toluene

2: tert-BuOK / toluene

3: AD-mix α; tert-BuOH / H2O

4: triethylamine / toluene

5: PTSA; acetic acid / H₂O

With AD-mix-α; potassium tert-butylate; toluene-4-sulfonic acid; acetic acid; triethylamine; tert-butyl alcohol; In water; toluene; 2: Wittig reaction / 3: Sharpless asymmetric dihydroxylation;
DOI:10.1016/S0040-4039(02)02662-X

Reference yield:

: 337903-22-7
3,5-O-(2-formylbenzylidene)-1,2-O-isopropylidene-α-D-xylofuranose

: 528584-56-7
Benzoic acid (1S,3S)-3-hydroxy-1,3-dihydro-isobenzofuran-1-ylmethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: tert-BuOK / toluene

2: AD-mix α; tert-BuOH / H2O

3: triethylamine / toluene

4: PTSA; acetic acid / H₂O

With AD-mix-α; potassium tert-butylate; toluene-4-sulfonic acid; acetic acid; triethylamine; tert-butyl alcohol; In water; toluene; 1: Wittig reaction / 2: Sharpless asymmetric dihydroxylation;
DOI:10.1016/S0040-4039(02)02662-X