(2S,4R,6S)-2-[2-(4-Benzyloxy-phenyl)-ethyl]-4-bromo-6-(4-chloro-phenyl)-tetrahydro-pyran

Base Information

Chemical Name:(2S,4R,6S)-2-[2-(4-Benzyloxy-phenyl)-ethyl]-4-bromo-6-(4-chloro-phenyl)-tetrahydro-pyran
CAS No.:477284-04-1
Molecular Formula:C₂₆H₂₆BrClO₂
Molecular Weight:485.848
Hs Code.:

Synonyms:(2S,4R,6S)-2-[2-(4-Benzyloxy-phenyl)-ethyl]-4-bromo-6-(4-chloro-phenyl)-tetrahydro-pyran

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Chemical Property of (2S,4R,6S)-2-[2-(4-Benzyloxy-phenyl)-ethyl]-4-bromo-6-(4-chloro-phenyl)-tetrahydro-pyran

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Technology Process of (2S,4R,6S)-2-[2-(4-Benzyloxy-phenyl)-ethyl]-4-bromo-6-(4-chloro-phenyl)-tetrahydro-pyran

There total 5 articles about (2S,4R,6S)-2-[2-(4-Benzyloxy-phenyl)-ethyl]-4-bromo-6-(4-chloro-phenyl)-tetrahydro-pyran 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: 89.0%

: 477284-13-2
Acetic acid 3-(4-benzyloxy-phenyl)-1-[(S)-1-(4-chloro-phenyl)-but-3-enyloxy]-propyl ester

: 477284-04-1
(2S,4R,6S)-2-[2-(4-Benzyloxy-phenyl)-ethyl]-4-bromo-6-(4-chloro-phenyl)-tetrahydro-pyran

Guidance literature:: With stannic bromide; In dichloromethane; at -78 ℃; for 1h;
DOI:10.1021/ol026751i

Reference yield: 73.0%

: 68486-77-1
3-(4-(benzyloxy)phenyl)propanal

: 14506-33-3,104869-96-7,132620-81-6
(S)-1-(4-chlorophenyl)-but-3-en-1-ol

: 477284-04-1
(2S,4R,6S)-2-[2-(4-Benzyloxy-phenyl)-ethyl]-4-bromo-6-(4-chloro-phenyl)-tetrahydro-pyran

Guidance literature:: With stannic bromide; In dichloromethane; at -78 - -30 ℃; for 24h;
DOI:10.1021/ol026751i

Reference yield:

: 104-88-1
4-chlorobenzaldehyde

: 477284-04-1
(2S,4R,6S)-2-[2-(4-Benzyloxy-phenyl)-ethyl]-4-bromo-6-(4-chloro-phenyl)-tetrahydro-pyran

Guidance literature:: Multi-step reaction with 4 steps

1: (S)-BINOL; Ti(O-iPr)4

2: 98 percent / DCC / DMAP / CH₂Cl₂ / 12 h / 25 °C

3: 93 percent / DIBAL-H; pyridine; DMAP / CH₂Cl₂; hexane / -78 - 0 °C

4: 89 percent / SnBr₄ / CH₂Cl₂ / 1 h / -78 °C

With pyridine; titanium(IV) isopropylate; dmap; (S)-[1,1']-binaphthalenyl-2,2'-diol; stannic bromide; diisobutylaluminium hydride; dicyclohexyl-carbodiimide; dmap; In hexane; dichloromethane; 1: Keck's allylation;
DOI:10.1021/ol026751i