Sulfuric Acid → HCID 15735707, compound

HRID 1086687Notes

Reaction equation

HRID 1086687 reaction equation
[CH2:1]([Mg]Br)[CH:2]=[CH2:3].[O:6]([CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH:22]=[O:23])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.S(=O)(=O)(O)O.C(=O)(O)[O-].[Na+]>C(OCC)C.O1CCCC1>[O:6]([CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH:22]([OH:23])[CH2:3][CH:2]=[CH2:1])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1

Participants

7

Reactant 4

HCID 1118Sulfuric AcidHCID 516892Sodium BicarbonateHCID 15735706HCID 15735706, compoundHCID 178455850HCID 178455850, compound

Product 1

HCID 15735707HCID 15735707, compoundYield 42%

Reagents, catalysts & solvents 2

HCID 3283Diethyl EtherSolventHCID 8028TetrahydrofuranSolvent

Procedure

To 85 ml of a 1M solution of allyl magnesium bromide in diethyl ether cooled in ice bath was added dropwise, under nitrogen, a solution of 20 g of 10-phenoxydecanal in 200 ml of dry tetrahydrofuran. The mixture was poured into 400 ml of ice and 30 ml of 9M sulfuric acid was added. Upon standing the mixture formed aqueous and organic layers. The organic layer was stirred for 15 min with solid sodium bicarbonate and concentrated. The aqueous layer was extracted with diethyl ether (2×200 ml) and the extracts were combined with the concentrated organic layer. The combined organics were washed with 300 ml of water and 300 ml of a half-saturated aqueous solution of sodium chloride, filtered, and concentrated. The residue was flash chromatographed utilizing as successive eluents 5% diethyl ether/hexane, 10% diethyl ether/hexane, and 25% diethyl ether/hexane to give 18.51 g (42%) of 13-phenoxy-1-tridecen-4-ol as a solid, m.p. 50°-52°.

Workup

  1. additionwas added dropwise, under nitrogen
  2. additionwas added
  3. customformed aqueous
  4. concentrationconcentrated
  5. extractionThe aqueous layer was extracted with diethyl ether (2×200 ml)
  6. washThe combined organics were washed with 300 ml of water and 300 ml of a half-saturated aqueous solution of sodium chloride
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customchromatographed

Sources & evidence

ORD record
ord-8283423f20f6429db010985854ebc1ff
Source dataset
uspto-grants-1991_07
Patent number
US05030733

Reaction notes

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