5-tert-Butyldimethylsilyloxymethyl-1-phenylsulfonylmethyl-2,6,6-trimethylcyclohex-1-ene

Base Information

Chemical Name:5-tert-Butyldimethylsilyloxymethyl-1-phenylsulfonylmethyl-2,6,6-trimethylcyclohex-1-ene
CAS No.:171504-26-0
Molecular Formula:C₂₃H₃₈O₃SSi
Molecular Weight:422.704
Hs Code.:

Synonyms:5-tert-Butyldimethylsilyloxymethyl-1-phenylsulfonylmethyl-2,6,6-trimethylcyclohex-1-ene

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Chemical Property of 5-tert-Butyldimethylsilyloxymethyl-1-phenylsulfonylmethyl-2,6,6-trimethylcyclohex-1-ene

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Technology Process of 5-tert-Butyldimethylsilyloxymethyl-1-phenylsulfonylmethyl-2,6,6-trimethylcyclohex-1-ene

There total 7 articles about 5-tert-Butyldimethylsilyloxymethyl-1-phenylsulfonylmethyl-2,6,6-trimethylcyclohex-1-ene 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

: (3-Benzenesulfonylmethyl-2,2,4-trimethyl-cyclohex-3-enyl)-methanol

: 171504-26-0
5-tert-Butyldimethylsilyloxymethyl-1-phenylsulfonylmethyl-2,6,6-trimethylcyclohex-1-ene

Guidance literature:: With dmap; triethylamine; In dichloromethane; for 12h; Ambient temperature;
DOI:10.1016/0040-4020(95)00565-P

Reference yield:

: 144067-40-3
Acetic acid 5-formyl-2,6,6-trimethyl-cyclohex-1-enylmethyl ester

: 171504-26-0
5-tert-Butyldimethylsilyloxymethyl-1-phenylsulfonylmethyl-2,6,6-trimethylcyclohex-1-ene

Guidance literature:: Multi-step reaction with 6 steps

1: NaBH₄ / methanol / 0 °C

2: DMAP; Et₃N / CH₂Cl₂ / 0 - 20 °C

3: DIBAL-H / diethyl ether / 0 °C

4: 95 percent / pyridine; Bu₃P / 9 h / 20 °C

5: oxone / tetrahydrofuran; methanol; H₂O / 4 h / 20 °C

6: DMAP; Et₃N / CH₂Cl₂ / 20 °C

With pyridine; dmap; Oxone; sodium tetrahydroborate; tributylphosphine; diisobutylaluminium hydride; triethylamine; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; 1: Reduction / 2: Etherification / 3: Reduction / 4: Substitution / 5: Oxidation / 6: Etherification;
DOI:10.1039/b005727o

Reference yield:

: 144066-82-0
Acetic acid 2-isopropenyl-3-methyl-but-2-enyl ester

: 171504-26-0
5-tert-Butyldimethylsilyloxymethyl-1-phenylsulfonylmethyl-2,6,6-trimethylcyclohex-1-ene

Guidance literature:: Multi-step reaction with 7 steps

1: 82 percent / BF₃*Et₂O / CH₂Cl₂ / -78 °C

2: NaBH₄ / methanol / 0 °C

3: DMAP; Et₃N / CH₂Cl₂ / 0 - 20 °C

4: DIBAL-H / diethyl ether / 0 °C

5: 95 percent / pyridine; Bu₃P / 9 h / 20 °C

6: oxone / tetrahydrofuran; methanol; H₂O / 4 h / 20 °C

7: DMAP; Et₃N / CH₂Cl₂ / 20 °C

With pyridine; dmap; Oxone; sodium tetrahydroborate; tributylphosphine; boron trifluoride diethyl etherate; diisobutylaluminium hydride; triethylamine; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; 1: Cycloaddition / 2: Reduction / 3: Etherification / 4: Reduction / 5: Substitution / 6: Oxidation / 7: Etherification;
DOI:10.1039/b005727o