Carbamic acid (1S,4R,5R)-5-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enyl ester

Base Information

Chemical Name:Carbamic acid (1S,4R,5R)-5-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enyl ester
CAS No.:184179-62-2
Molecular Formula:C₂₀H₃₁NO₄Si
Molecular Weight:377.556
Hs Code.:

Synonyms:Carbamic acid (1S,4R,5R)-5-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enyl ester

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Chemical Property of Carbamic acid (1S,4R,5R)-5-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enyl ester

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Technology Process of Carbamic acid (1S,4R,5R)-5-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enyl ester

There total 6 articles about Carbamic acid (1S,4R,5R)-5-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enyl 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: 96.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 184179-61-1
Carbamic acid (1S,4R,5S)-5-benzyloxymethyl-4-hydroxy-cyclopent-2-enyl ester

: 184179-62-2
Carbamic acid (1S,4R,5R)-5-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enyl ester

Guidance literature:: With 1H-imidazole; In dichloromethane;
DOI:10.1021/ja960526c

Reference yield:

: 100021-11-2
(1α,2β,3α)-2-(benzyloxymethyl)cyclopent-4-ene-1,3-diol

: 184179-62-2
Carbamic acid (1S,4R,5R)-5-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 89 percent / triethylamine, DMAP / CH₂Cl₂ / 1 h

2: 95 percent / NaH₂PO₄ buffer, aq. sodium azide / 144 h / electric eel acetylcholinesterase

3: pyridine

4: methanolic ammonia

5: K₂CO₃

6: 96 percent / imidazole / CH₂Cl₂

With pyridine; 1H-imidazole; dmap; sodium azide; NaH₂PO₄ buffer; ammonia; potassium carbonate; triethylamine; In dichloromethane;
DOI:10.1021/ja960526c

Reference yield:

: 134756-62-0
<1(S)-(1α,4α,5β)>-4-(acetyloxy)-5-<(benzyloxy)methyl>-2-cyclopenten-1-ol

: 184179-62-2
Carbamic acid (1S,4R,5R)-5-benzyloxymethyl-4-(tert-butyl-dimethyl-silanyloxy)-cyclopent-2-enyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine

2: methanolic ammonia

3: K₂CO₃

4: 96 percent / imidazole / CH₂Cl₂

With pyridine; 1H-imidazole; ammonia; potassium carbonate; In dichloromethane;
DOI:10.1021/ja960526c