Ethyl diazoacetate → 7-Hydroxy-6-propionyl-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-1-carboxylic acid ethyl ester

HRID 606334

Reaction equation

HRID 606334 reaction equation
[OH:1][C:2]1[C:11]([C:12](=[O:15])[CH2:13][CH3:14])=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH2:6][O:7]2.[N+](=[CH:18][C:19]([O:21][CH2:22][CH3:23])=[O:20])=[N-]>ClCCCl>[CH2:22]([O:21][C:19]([CH:18]1[CH:4]2[CH:5]1[CH2:6][O:7][C:8]1[CH:9]=[CH:10][C:11]([C:12](=[O:15])[CH2:13][CH3:14])=[C:2]([OH:1])[C:3]=12)=[O:20])[CH3:23]

Participants

4

Reactant 2

HCID 12192Ethyl diazoacetateHCID 224828711-(5-hydroxy-2H-chromen-6-yl)-propan-1-one

Product 1

HCID 213049647-Hydroxy-6-propionyl-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-1-carboxylic acid ethyl esterYield 41.3%

Reagents, catalysts & solvents 1

HCID 111,2-DichloroethaneSolvent2×

Procedure

To a mixture of 1-(5-hydroxy-2H-chromen-6-yl)-propan-1-one (511 mg, 2.5 mmol) and (Rh(II)Ac2)2 (11 mg, 0.025 mmol) in 1,2-dichloroethane (8 mL) at 20° C., was added dropwise (3 h) a solution of ethyl diazoacetate (571 mg, 5 mmol) in 1,2-dichloroethane (2 mL). After 15 min at 20° C., the reaction mixture was washed with H2O (10 mL). The H2O phase was washed with CH2Cl2 (10 mL) and the solvent of the combined organic phases was removed under reduced pressure. The crude product was purified by column chromatography (silica gel, 1→5% MeOH in CH2Cl2), to give 300 mg (41%) of 7-hydroxy-6-propionyl-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-1-carboxylic acid ethyl ester (a 33/64 mixture of cis and trans isomers).

Workup

  1. washthe reaction mixture was washed with H2O (10 mL)
  2. washThe H2O phase was washed with CH2Cl2 (10 mL)
  3. customthe solvent of the combined organic phases was removed under reduced pressure
  4. customThe crude product was purified by column chromatography (silica gel, 1→5% MeOH in CH2Cl2)

Sources & evidence

ORD record
ord-2f3780e072e9422cbddb27c5267d98c8
Source dataset
uspto-grants-2011_03
Patent number
US07915295B2

Linked notes

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