Ammonium Carbonate → HCID 10293759, compound

HRID 1071858Notes

Reaction equation

HRID 1071858 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-4e3fe2752b9a45ae87683ba9f1c6408b
Source dataset
uspto-grants-2005_06
Patent number
US06906206B2

Reaction notes

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