Cas no 864943-23-7 ((R)-4-oxide-4-hydroxy-2,6-di-1-naphthalenyl-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin)

(R)-4-oxide-4-hydroxy-2,6-di-1-naphthalenyl-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin structure
864943-23-7 structure
Product Name:(R)-4-oxide-4-hydroxy-2,6-di-1-naphthalenyl-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
CAS No:864943-23-7
MF:C40H25O4P
MW:600.597871541977
CID:2360887
Update Time:2024-10-26

(R)-4-oxide-4-hydroxy-2,6-di-1-naphthalenyl-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin Chemical and Physical Properties

Names and Identifiers

    • (R)-4-oxide-4-hydroxy-2,6-di-1-naphthalenyl-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
    • R-4-OXIDE-4-HYDROXY-2,6-DI-1-NAPHTHALENYL-DINAPHTHO[2,1-D:1',2'-F][1,3,2]DIOXAPHOSPHEPIN
    • (11bR)-4-Hydroxy-2,6-di-1-naphthalenyl-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
    • (R)-3,3′-Bis(1-naphthyl)-1,1′-binaphthalene-2,2′-diyl hydrogen phosphate
    • Inchi: 1S/C40H25O4P/c41-45(42)43-39-35(33-21-9-15-25-11-1-5-17-29(25)33)23-27-13-3-7-19-31(27)37(39)38-32-20-8-4-14-28(32)24-36(40(38)44-45)34-22-10-16-26-12-2-6-18-30(26)34/h1-24H,(H,41,42)
    • InChI Key: SLYOKZNBLPQLJA-UHFFFAOYSA-N
    • SMILES: O=P1(OC2C(C3C4C(=CC=CC=4)C=CC=3)=CC3C(C=2C2C(=C(C4C5C(=CC=CC=5)C=CC=4)C=C4C=2C=CC=C4)O1)=CC=CC=3)O

(R)-4-oxide-4-hydroxy-2,6-di-1-naphthalenyl-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin Pricemore >>

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abcr
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(11bR)-4-Hydroxy-2,6-di-1-naphthalenyl-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin, 98%, (99% ee); .
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(R)-4-oxide-4-hydroxy-2,6-di-1-naphthalenyl-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Phosphorus oxychloride Solvents: Pyridine ;  0 °C; 10 min, 0 °C; 12 h, 98 °C; 98 °C → rt
1.2 Solvents: Water ;  rt; 6 h, 98 °C; 98 °C → rt
1.3 Reagents: Hydrochloric acid Solvents: Dichloromethane ,  Water ;  15 min, rt
Reference
Bronsted Acid-Catalyzed Regioselective Carboxamidation of 2-Indolylmethanols with Isonitriles
Chaudhari, Tohasib Yusub; et al, Journal of Organic Chemistry, 2023, 88(15), 10412-10425

Production Method 2

Reaction Conditions
1.1 Reagents: Phosphorus oxychloride Solvents: Pyridine ;  rt; rt → 95 °C; 12 h, 95 °C; 95 °C → 0 °C
1.2 Reagents: Water ;  0 °C; 6 h, 0 °C → 95 °C
Reference
Chiral lithium salts of phosphoric acids as lewis acid-base conjugate catalysts for the enantioselective cyanosilylation of ketones
Hatano, Manabu; et al, Advanced Synthesis & Catalysis, 2008, 350, 1776-1780

Production Method 3

Reaction Conditions
1.1 Reagents: Pyridine ,  Phosphorus oxychloride ;  18 h, rt
1.2 Reagents: Triethylamine Solvents: Dichloromethane ,  Water ;  4 h, rt
Reference
Chiral Counteranion-Directed Catalytic Asymmetric Methylene Migration Reaction of Ene-Aldimines
Momiyama, Norie ; et al, Journal of Organic Chemistry, 2022, 87(14), 9399-9407

(R)-4-oxide-4-hydroxy-2,6-di-1-naphthalenyl-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin Raw materials

(R)-4-oxide-4-hydroxy-2,6-di-1-naphthalenyl-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin Preparation Products

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