Ammonium Carbonate → HCID 10293759, compound

HRID 496044Notes

Reaction equation

HRID 496044 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([O:11][CH2:12][C@H:13]2[CH2:27][O:26][C:16]3[CH:17]=[CH:18][C:19]4[C:20](=[O:25])[CH:21]=[CH:22][O:23][C:24]=4[C:15]=3[O:14]2)(=[O:10])=[O:9])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[NH4+].[NH4+]>CO.[Pd]>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([S:8]([O:11][CH2:12][CH:13]2[CH2:27][O:26][C:16]3[CH:17]=[CH:18][C:19]4[C:20](=[O:25])[CH2:21][CH2:22][O:23][C:24]=4[C:15]=3[O:14]2)(=[O:10])=[O:9])=[CH:6][CH:7]=1

Participants

5

Procedure

0.50 g (1.28 mmole) of [(2R)-7-oxo-2,3-dihydro-7H-[1,4]dioxino[2,3-h]chromen-2-yl]methyl 4-methylbenzenesulfonate in methanol was added to a round bottom flask containing 0.40 g of 10% palladium on carbon under a stream of nitrogen, ammonium carbonate was then added and the heterogeneous mixture was heated to reflux for 2.5 hours. After the catalyst was removed by filtration, the filtrate was concentrated in vacuum and the residue column chromatographed on silica gel with 0.5% methanol/methylene chloride as eluant to give 0.30 g (61%) of the (R)-enantiomer of the title compound as a white foam. 1H (CDCl3) doublet 7.8 δ (2H); doublet 7.5 δ (1H); doublet 7.4 δ (2H); doublet 6.6 δ (1H); triplet 4.6 δ (2H); multiplet 4-4.5 δ (5H); triplet 2.8 δ (2H); singlet 2.5 δ (3H).

Workup

  1. additionwas then added
  2. temperaturethe heterogeneous mixture was heated
  3. temperatureto reflux for 2.5 hours
  4. customAfter the catalyst was removed by filtration
  5. concentrationthe filtrate was concentrated in vacuum
  6. customthe residue column chromatographed on silica gel with 0.5% methanol/methylene chloride as eluant

Sources & evidence

ORD record
ord-c40b3970bb084edc885bfb989d391c08
Source dataset
uspto-grants-2005_09
Patent number
US06943178B2

Reaction notes

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