Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-tert-Butyl-5-methyl-2-(propan-2-yl)phenol | HCID 14618371 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 14618373 | HCID 14618373 | 8.6% |
Reaction Steps
A mixture of 4-(1,1-dimethylethyl)-2-(1-methylethyl)-5-methylphenol (103.2 g, 0.5 mol), 40% formaldehyde solution (375 mL, 5 mol), potassium hydroxide (49.5 g, 0.75 mol) and poly(ethylene glycol) avg. M.W. 300 (1 g) was heated at reflux for 24 hour. The mixture was cooled to 25° C. and water (1 L) and hexane (700 mL) were added. The aqueous layer was extracted with hexane (2×100 mL). The combined organic extracts were washed with water (3×100 mL), brine (2×100 mL) and dried (Na2SO4). Evaporation of solvents and crystallization of the residue from hexane gave 10.2 g (8.6% yield) of 5-(1,1-dimethylethyl)-6-methyl-3-(1-methylethyl)-2-hydroxy benzenemethanol, mp 143°-146° C.; 1H-NMR (CDCl3)δ 1.25 (6H, d, J=7 Hz), 1.40 (9H, s), 2.31 (3H, s), 3.0-3.6 (1H, m), 4.85 (2H, s), 7.01 (1H, s), 7.23 (1H, s); IR (CHCl3)νmax 3550, 3350, 2940, 1575, 1470, 1360 cm-1 ; M m/e 236, 218, 206, 203, 191, 161, UVλmax (ethanol) 224 nm (ε=6690), 287 nm (ε=2480).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04880775 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-1b546a94562e4dff8efe9d1355805cb2 |
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| Source note | uspto-grants-1989_11 |
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