Hydrochloric Acid → HCID 15287673, compound

HRID 1741686Notes

Reaction equation

HRID 1741686 reaction equation
[CH3:1][C:2]([C:5]1[CH:10]=[C:9]([SH:11])[CH:8]=[C:7]([C:12]([CH3:15])([CH3:14])[CH3:13])[C:6]=1[OH:16])([CH3:4])[CH3:3].[O-]CC.[Na+].[CH:21]12[O:27][CH:22]1[CH2:23][CH2:24][CH2:25][CH2:26]2.Cl>C(O)C>[CH3:13][C:12]([C:7]1[CH:8]=[C:9]([S:11][C@@H:21]2[CH2:26][CH2:25][CH2:24][CH2:23][C@H:22]2[OH:27])[CH:10]=[C:5]([C:2]([CH3:1])([CH3:3])[CH3:4])[C:6]=1[OH:16])([CH3:15])[CH3:14]

Participants

6

Procedure

2,6-bis(1,1-Dimethylethyl)-4-mercaptophenol (12.8 g, 0.054 moles) was added to a solution of sodium ethoxide [prepared from sodium (2.5 g, 0.108 mole)] in ethyl alcohol (75 ml). Cyclohexene oxide (5.15 g, 0.0525 mole) was added and the reaction mixture was stirred at room temperature for 20 hours. The reaction mixture was poured into 10% hydrochloric acid (250 ml) and the mixture was extracted twice with 200 ml of ethyl ether. The combined ethyl ether extracts were washed twice with 25 ml of water, dried over magnesium sulfate, filtered and concentrated in vacuo to a yellow oil. The product was purified by silica get chromatography and recrystallized from methyl alcohol/water, m.p. ca 91° C. The structure was supported by NMR, infrared spectroscopy, and elemental analysis.

Workup

  1. extractionthe mixture was extracted twice with 200 ml of ethyl ether
  2. washThe combined ethyl ether extracts were washed twice with 25 ml of water
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo to a yellow oil
  6. customThe product was purified by silica
  7. customget chromatography
  8. customrecrystallized from methyl alcohol/water, m.p. ca 91° C

Sources & evidence

ORD record
ord-c65c8db64f794bbb946e561a8cc2866d
Source dataset
uspto-grants-1994_08
Patent number
US05334616

Reaction notes

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