(2R)-8-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl-4-methylbenzenesulfonate

Base Information

Chemical Name:(2R)-8-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl-4-methylbenzenesulfonate
CAS No.:137309-89-8
Molecular Formula:C₁₇H₁₈O₆S
Molecular Weight:350.392
Hs Code.:

Synonyms:(2R)-8-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl-4-methylbenzenesulfonate

Suppliers and Price of (2R)-8-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl-4-methylbenzenesulfonate

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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 (2R)-8-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl-4-methylbenzenesulfonate

Chemical Property:

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Technology Process of (2R)-8-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl-4-methylbenzenesulfonate

There total 5 articles about (2R)-8-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl-4-methylbenzenesulfonate 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: 81.0%

: 122450-20-8
2-benzyloxy-3-methoxyphenol

: 137309-89-8
(2R)-8-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl-4-methylbenzenesulfonate

Guidance literature:

Reference yield:

: 98-59-9
p-toluenesulfonyl chloride

: 99186-65-9
(R,S)-(8-methoxy-2,3-dihydro-1,4-benzodioxin-2-yl)methanol

: 137309-89-8
(2R)-8-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl-4-methylbenzenesulfonate

Guidance literature:: With pyridine; at 20 ℃;
DOI:10.1021/jm9910122

Reference yield:

: 70918-44-4
8-methoxy-2,3-dihydro-1,4-benzodioxin-2-carboxamide

: 137309-89-8
(2R)-8-methoxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl-4-methylbenzenesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: HCl / 16 h / Heating

2: LiAlH₄ / diethyl ether / 2 h / 20 °C

3: pyridine / 20 °C

With pyridine; hydrogenchloride; lithium aluminium tetrahydride; In diethyl ether; 1: ethanolysis / 2: Reduction / 3: tosylation;
DOI:10.1021/jm9910122