4-hydroxymethyl-5-(5-isopropenyl-2-methyl-1-en-cyclopentyl)-3-phenthiomethyl-dihydrofuran-2(3H)-one

Base Information

Chemical Name:4-hydroxymethyl-5-(5-isopropenyl-2-methyl-1-en-cyclopentyl)-3-phenthiomethyl-dihydrofuran-2(3H)-one
CAS No.:1376595-59-3
Molecular Formula:C₂₁H₂₆O₃S
Molecular Weight:358.502
Hs Code.:

Synonyms:4-hydroxymethyl-5-(5-isopropenyl-2-methyl-1-en-cyclopentyl)-3-phenthiomethyl-dihydrofuran-2(3H)-one

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Chemical Property of 4-hydroxymethyl-5-(5-isopropenyl-2-methyl-1-en-cyclopentyl)-3-phenthiomethyl-dihydrofuran-2(3H)-one

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Technology Process of 4-hydroxymethyl-5-(5-isopropenyl-2-methyl-1-en-cyclopentyl)-3-phenthiomethyl-dihydrofuran-2(3H)-one

There total 3 articles about 4-hydroxymethyl-5-(5-isopropenyl-2-methyl-1-en-cyclopentyl)-3-phenthiomethyl-dihydrofuran-2(3H)-one 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: 88.0%

: 4-hydroxymethyl-5-(5-isopropenyl-2-methyl-1-en-cyclopentyl)-3-methylenedihydrofuran-2(3H)-one

: 108-98-5
thiophenol

: 1376595-59-3
4-hydroxymethyl-5-(5-isopropenyl-2-methyl-1-en-cyclopentyl)-3-phenthiomethyl-dihydrofuran-2(3H)-one

Guidance literature:: With dmap; In dichloromethane; at 20 ℃; for 3h; Cooling with ice;
DOI:10.1039/c2ob25397f

Reference yield:

: 58588-90-2
α-bromomethyl-γ-butene lactone

: 1376595-59-3
4-hydroxymethyl-5-(5-isopropenyl-2-methyl-1-en-cyclopentyl)-3-phenthiomethyl-dihydrofuran-2(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: ammonium chloride; zinc / tetrahydrofuran; water / 0.25 h / 20 °C

2.1: alkali hydroxide / tetrahydrofuran; water / 2.5 h / 20 °C

2.2: pH 1

3.1: dmap / dichloromethane / 3 h / 20 °C / Cooling with ice

With dmap; ammonium chloride; zinc; In tetrahydrofuran; dichloromethane; water; 1.1: Barbier reaction / 2.1: Barbier reaction / 3.1: Barbier reaction;
DOI:10.1039/c2ob25397f

Reference yield:

: 3865-09-6,38231-11-7,83945-83-9,93221-52-4
(R)-2-methyl-5-(prop-1-en-2-yl)cyclopent-1-ene-1-carbaldehyde

: 1376595-59-3
4-hydroxymethyl-5-(5-isopropenyl-2-methyl-1-en-cyclopentyl)-3-phenthiomethyl-dihydrofuran-2(3H)-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: ammonium chloride; zinc / tetrahydrofuran; water / 0.25 h / 20 °C

2.1: alkali hydroxide / tetrahydrofuran; water / 2.5 h / 20 °C

2.2: pH 1

3.1: dmap / dichloromethane / 3 h / 20 °C / Cooling with ice

With dmap; ammonium chloride; zinc; In tetrahydrofuran; dichloromethane; water; 1.1: Barbier reaction / 2.1: Barbier reaction / 3.1: Barbier reaction;
DOI:10.1039/c2ob25397f