(R,S)-5-[(R)-(benzyloxymethyl)(tert-butanesulfinylamino)methyl]furan-2(4H)-one

Base Information

Chemical Name:(R,S)-5-[(R)-(benzyloxymethyl)(tert-butanesulfinylamino)methyl]furan-2(4H)-one
CAS No.:1329451-14-0
Molecular Formula:C₁₇H₂₅NO₄S
Molecular Weight:339.456
Hs Code.:

Synonyms:(R,S)-5-[(R)-(benzyloxymethyl)(tert-butanesulfinylamino)methyl]furan-2(4H)-one

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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 (R,S)-5-[(R)-(benzyloxymethyl)(tert-butanesulfinylamino)methyl]furan-2(4H)-one

Chemical Property:

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Technology Process of (R,S)-5-[(R)-(benzyloxymethyl)(tert-butanesulfinylamino)methyl]furan-2(4H)-one

There total 3 articles about (R,S)-5-[(R)-(benzyloxymethyl)(tert-butanesulfinylamino)methyl]furan-2(4H)-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: 92.0%

: 1329450-98-7
(R_S,5R)-5-[(1S)-(benzyloxymethyl)(tert-butylsulfinylamino)methyl]furan-2(5H)-one

: 1329451-14-0
(R,S)-5-[(R)-(benzyloxymethyl)(tert-butanesulfinylamino)methyl]furan-2(4H)-one

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In ethyl acetate; for 20h;
DOI:10.1021/ol2020384

Reference yield:

: 60656-87-3
benzyloxyacetoaldehyde

: 1329451-14-0
(R,S)-5-[(R)-(benzyloxymethyl)(tert-butanesulfinylamino)methyl]furan-2(4H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: pyridinium p-toluenesulfonate; magnesium sulfate / dichloromethane / 20 h / 20 °C

2: trimethylsilyl trifluoromethanesulfonate / dichloromethane / 1 h / -78 °C / Inert atmosphere

3: palladium 10% on activated carbon; hydrogen / ethyl acetate / 20 h

With trimethylsilyl trifluoromethanesulfonate; palladium 10% on activated carbon; hydrogen; pyridinium p-toluenesulfonate; magnesium sulfate; In dichloromethane; ethyl acetate; 2: Mannich reaction;
DOI:10.1021/ol2020384

Reference yield:

: 393536-17-9
(R)-N-[(1E)-2-(benzyloxy)ethylidene]-2-methylpropane-2-sulfinamide

: 1329451-14-0
(R,S)-5-[(R)-(benzyloxymethyl)(tert-butanesulfinylamino)methyl]furan-2(4H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: trimethylsilyl trifluoromethanesulfonate / dichloromethane / 1 h / -78 °C / Inert atmosphere

2: palladium 10% on activated carbon; hydrogen / ethyl acetate / 20 h

With trimethylsilyl trifluoromethanesulfonate; palladium 10% on activated carbon; hydrogen; In dichloromethane; ethyl acetate; 1: Mannich reaction;
DOI:10.1021/ol2020384