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30508-27-1

Basic Information
CAS No.: 30508-27-1
Name: licoricidin
Molecular Structure:
Molecular Structure of 30508-27-1 (licoricidin)
Formula: C26H32 O5
Molecular Weight: 424.537
Synonyms: 1,3-Benzenediol,4-[(3R)-3,4-dihydro-7-hydroxy-5-methoxy-6-(3-methyl-2-butenyl)-2H-1-benzopyran-3-yl]-2-(3-methyl-2-butenyl)-(9CI); 1,3-Benzenediol,4-[3,4-dihydro-7-hydroxy-5-methoxy-6-(3-methyl-2-butenyl)-2H-1-benzopyran-3-yl]-2-(3-methyl-2-butenyl)-,(R)-; 2',4',5-Isoflavantriol, 7-methoxy-3',6-bis(3-methyl-2-butenyl)- (8CI);(+)-Licoricidin; 7-O-Demethyllicorisoflavan A; Licoricidin; Licorisoflavan B
Density: 1.171g/cm3
Melting Point: 161.0-162.5℃
Boiling Point: 610.8°Cat760mmHg
Flash Point: 323.2°C
PSA: 79.15000
LogP: 5.54810
Synthetic route
30508-27-1

(+)-(R)-licoricidin

77-78-1

dimethyl sulfate

6-[(R)-5,7-Dimethoxy-6-(3-methyl-but-2-enyl)-chroman-3-yl]-3-methoxy-2-(3-methyl-but-2-enyl)-phenol

Conditions
ConditionsYield
With potassium carbonate In acetone
108-24-7

acetic anhydride

30508-27-1

(+)-(R)-licoricidin

(+)-(R)-licoricidin triacetate

Conditions
ConditionsYield
In pyridine
30508-27-1

(+)-(R)-licoricidin

A

6-((R)-5-Methoxy-8,8-dimethyl-3,4,7,8-tetrahydro-2H,6H-pyrano[3,2-g]chromen-3-yl)-2,2-dimethyl-chroman-5-ol

B

8-((R)-5-Methoxy-8,8-dimethyl-3,4,7,8-tetrahydro-2H,6H-pyrano[3,2-g]chromen-3-yl)-2,2-dimethyl-chroman-5-ol

Conditions
ConditionsYield
With hydrogenchloride In methanol
30508-27-1

(+)-(R)-licoricidin

1346768-14-6

4',7-dihydroxy-5-methoxy-6,3'-diprenylisoflavanquinone

Conditions
ConditionsYield
With sodium hydroxide In ethanol for 2h;
30508-27-1

(+)-(R)-licoricidin

C30H34O7

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: pyridine / 16 h
2: palladium dichloride / ethanol; water / 48 h / 20 °C
View Scheme
30508-27-1

(+)-(R)-licoricidin

A

1006718-45-1

1-methoxyerythrabyssin II

B

1551035-71-2

licorisoflavan D

Conditions
ConditionsYield
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In benzene for 0.0833333h; Reflux;A 1 mg
B 9.9 mg
30508-27-1

(+)-(R)-licoricidin

A

1551035-46-1

licorisoflavan C

B

1551035-71-2

licorisoflavan D

C

licorisoflavan E

Conditions
ConditionsYield
With palladium dichloride In ethanol at 20℃; for 4h;A 5.2 mg
B 3.2 mg
C 7.6 mg
30508-27-1

(+)-(R)-licoricidin

licorisoflavan E

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: pyridine / 16 h
2: palladium dichloride / ethanol; water / 48 h / 20 °C
3: sodium hydroxide; water / 0.5 h
View Scheme
108-24-7

acetic anhydride

30508-27-1

(+)-(R)-licoricidin

A

1542237-27-3

7,2'-diacetyllicoricidin

B

1542237-28-4

7,4'-diacetyllicoricidin

C

1542237-29-5

2',4'-diacetyllicoricidin

Conditions
ConditionsYield
With pyridine for 16h;A 24.2 mg
B 6.7 mg
C 54.6 mg
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