(+)-phenylselenyl [(4aS,8R,8aS)-7-phenylthio-1,1,6-trimethyl-8-(4-methoxyphenylsulfonyl)-1,3,4,5,8,8a-hexahydronaphthalen-4a(2H)-yl]acetate

Base Information

Chemical Name:(+)-phenylselenyl [(4aS,8R,8aS)-7-phenylthio-1,1,6-trimethyl-8-(4-methoxyphenylsulfonyl)-1,3,4,5,8,8a-hexahydronaphthalen-4a(2H)-yl]acetate
CAS No.:674781-49-8
Molecular Formula:C₃₄H₃₈O₄S₂Se
Molecular Weight:653.765
Hs Code.:

Synonyms:(+)-phenylselenyl [(4aS,8R,8aS)-7-phenylthio-1,1,6-trimethyl-8-(4-methoxyphenylsulfonyl)-1,3,4,5,8,8a-hexahydronaphthalen-4a(2H)-yl]acetate

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Chemical Property of (+)-phenylselenyl [(4aS,8R,8aS)-7-phenylthio-1,1,6-trimethyl-8-(4-methoxyphenylsulfonyl)-1,3,4,5,8,8a-hexahydronaphthalen-4a(2H)-yl]acetate

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Technology Process of (+)-phenylselenyl [(4aS,8R,8aS)-7-phenylthio-1,1,6-trimethyl-8-(4-methoxyphenylsulfonyl)-1,3,4,5,8,8a-hexahydronaphthalen-4a(2H)-yl]acetate

There total 10 articles about (+)-phenylselenyl [(4aS,8R,8aS)-7-phenylthio-1,1,6-trimethyl-8-(4-methoxyphenylsulfonyl)-1,3,4,5,8,8a-hexahydronaphthalen-4a(2H)-yl]acetate 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: 71.0%

: 645-96-5
Benzeneselenol

: 674781-60-3
(+)-[(4aS,8R,8aS)-7-phenylthio-1,1,6-trimethyl-8-(4-methoxyphenylsulfonyl)-1,3,4,5,8,8a-hexahydronaphthalen-4a(2H)-yl]acetic acid

: 674781-49-8
(+)-phenylselenyl [(4aS,8R,8aS)-7-phenylthio-1,1,6-trimethyl-8-(4-methoxyphenylsulfonyl)-1,3,4,5,8,8a-hexahydronaphthalen-4a(2H)-yl]acetate

Guidance literature:: (+)-[(4aS,8R,8aS)-7-phenylthio-1,1,6-trimethyl-8-(4-methoxyphenylsulfonyl)-1,3,4,5,8,8a-hexahydronaphthalen-4a(2H)-yl]acetic acid; With O-phenyl phosphorodichloridate; triethylamine; In tetrahydrofuran; at 0 ℃; for 1h;

Benzeneselenol; With triethylamine; In tetrahydrofuran; at 0 ℃; for 0.5h;
DOI:10.1021/ol0363063

Reference yield:

: 166022-29-3
(S)-(+)-(2',2'-dimethyl-6'-methylene-1'-cyclohexyl)methanol

: 674781-49-8
(+)-phenylselenyl [(4aS,8R,8aS)-7-phenylthio-1,1,6-trimethyl-8-(4-methoxyphenylsulfonyl)-1,3,4,5,8,8a-hexahydronaphthalen-4a(2H)-yl]acetate

Guidance literature:: Multi-step reaction with 9 steps

1.1: oxalyl chloride; DMSO; Et₃N / CH₂Cl₂ / -78 - 20 °C

2.1: Mg / tetrahydrofuran

2.2: tetrahydrofuran / 0.5 h / 0 °C

2.3: 2.5 g / HMPA / tetrahydrofuran / 0 - 20 °C

3.1: 57 percent / PPh₃; AcOH / Pd(OAc)2 / 760 Torr / Heating

4.1: 92 percent / K₂CO₃ / acetone / 4 h / 20 °C

5.1: 78 percent / aq. NaOH; benzyltriethylammonium chloride; MeOH / CH₂Cl₂ / 8 h / 20 °C

6.1: 99 percent / 1,1,1,3,3,3-hexafluoro-2-propanol; NaHCO₃ / 4 h / 20 °C

7.1: 97 percent / m-CPBA; NaHCO₃ / CH₂Cl₂ / 4 h / 20 °C

8.1: 100 percent / aq. NaOH / H₂O / 6 h / Heating

9.1: Et₃N; PhOP(O)Cl₂ / tetrahydrofuran / 1 h / 0 °C

9.2: 71 percent / Et₃N / tetrahydrofuran / 0.5 h / 0 °C

With methanol; sodium hydroxide; oxalyl dichloride; 1,1,1,3',3',3'-hexafluoro-propanol; N-benzyl-N,N,N-triethylammonium chloride; sodium hydrogencarbonate; potassium carbonate; magnesium; acetic acid; dimethyl sulfoxide; O-phenyl phosphorodichloridate; triethylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; palladium diacetate; In tetrahydrofuran; dichloromethane; water; acetone; 1.1: Swern oxidation;
DOI:10.1021/ol0363063

Reference yield:

: 166022-30-6
(S)-(+)-2',2'-dimethyl-6'-methylene-1'-cyclohexylcarboxaldehyde

: 674781-49-8
(+)-phenylselenyl [(4aS,8R,8aS)-7-phenylthio-1,1,6-trimethyl-8-(4-methoxyphenylsulfonyl)-1,3,4,5,8,8a-hexahydronaphthalen-4a(2H)-yl]acetate

Guidance literature:: Multi-step reaction with 8 steps

1.1: Mg / tetrahydrofuran

1.2: tetrahydrofuran / 0.5 h / 0 °C

1.3: 2.5 g / HMPA / tetrahydrofuran / 0 - 20 °C

2.1: 57 percent / PPh₃; AcOH / Pd(OAc)2 / 760 Torr / Heating

3.1: 92 percent / K₂CO₃ / acetone / 4 h / 20 °C

4.1: 78 percent / aq. NaOH; benzyltriethylammonium chloride; MeOH / CH₂Cl₂ / 8 h / 20 °C

5.1: 99 percent / 1,1,1,3,3,3-hexafluoro-2-propanol; NaHCO₃ / 4 h / 20 °C

6.1: 97 percent / m-CPBA; NaHCO₃ / CH₂Cl₂ / 4 h / 20 °C

7.1: 100 percent / aq. NaOH / H₂O / 6 h / Heating

8.1: Et₃N; PhOP(O)Cl₂ / tetrahydrofuran / 1 h / 0 °C

8.2: 71 percent / Et₃N / tetrahydrofuran / 0.5 h / 0 °C

With methanol; sodium hydroxide; 1,1,1,3',3',3'-hexafluoro-propanol; N-benzyl-N,N,N-triethylammonium chloride; sodium hydrogencarbonate; potassium carbonate; magnesium; acetic acid; O-phenyl phosphorodichloridate; triethylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; palladium diacetate; In tetrahydrofuran; dichloromethane; water; acetone;
DOI:10.1021/ol0363063