(R)-N-[1-(tert-butyldimethylsilyloxymethyl)but-3-ynyl]-4-methylbenzenesulfonamide

Base Information

Chemical Name:(R)-N-[1-(tert-butyldimethylsilyloxymethyl)but-3-ynyl]-4-methylbenzenesulfonamide
CAS No.:437553-86-1
Molecular Formula:C₁₈H₂₉NO₃SSi
Molecular Weight:367.585
Hs Code.:

Synonyms:(R)-N-[1-(tert-butyldimethylsilyloxymethyl)but-3-ynyl]-4-methylbenzenesulfonamide

Suppliers and Price of (R)-N-[1-(tert-butyldimethylsilyloxymethyl)but-3-ynyl]-4-methylbenzenesulfonamide

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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)-N-[1-(tert-butyldimethylsilyloxymethyl)but-3-ynyl]-4-methylbenzenesulfonamide

Chemical Property:

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Technology Process of (R)-N-[1-(tert-butyldimethylsilyloxymethyl)but-3-ynyl]-4-methylbenzenesulfonamide

There total 4 articles about (R)-N-[1-(tert-butyldimethylsilyloxymethyl)but-3-ynyl]-4-methylbenzenesulfonamide 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: 80.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 437553-84-9
(R)-N-(1-hydroxymethylbut-3-ynyl)-4-methylbenzenesulfonamide

: 437553-86-1
(R)-N-[1-(tert-butyldimethylsilyloxymethyl)but-3-ynyl]-4-methylbenzenesulfonamide

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 35 ℃; for 2.5h;
DOI:10.1002/1615-4169(200201)344:1<70::AID-ADSC70>3.0.CO;2-1

Reference yield:

: 23235-01-0,23235-03-2,50428-03-0,64165-64-6
(R)-2-aminopent-4-ynoic acid

: 437553-86-1
(R)-N-[1-(tert-butyldimethylsilyloxymethyl)but-3-ynyl]-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / aq. NaOH / 16 h / 20 °C

2: 100 percent / LiAlH₄ / tetrahydrofuran / 16 h / 20 °C

3: 80 percent / imidazole / dimethylformamide / 2.5 h / 35 °C

With 1H-imidazole; sodium hydroxide; lithium aluminium tetrahydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1002/1615-4169(200201)344:1<70::AID-ADSC70>3.0.CO;2-1

Reference yield:

: 98-59-9
p-toluenesulfonyl chloride

: 437553-86-1
(R)-N-[1-(tert-butyldimethylsilyloxymethyl)but-3-ynyl]-4-methylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 83 percent / aq. NaOH / 16 h / 20 °C

2: 100 percent / LiAlH₄ / tetrahydrofuran / 16 h / 20 °C

3: 80 percent / imidazole / dimethylformamide / 2.5 h / 35 °C

With 1H-imidazole; sodium hydroxide; lithium aluminium tetrahydride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1002/1615-4169(200201)344:1<70::AID-ADSC70>3.0.CO;2-1