Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dihydroxybenzophenone | HCID 8572 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-Benzenediol, 4-(phenylmethyl)- | HCID 75294 | — |
Reaction Steps
Triethyl amine (10 ml, 72.2 mmol) was added to a solution of 2,4-dihydroxybenzophenone (1) (5.4 g, 23.3 mmol) in THF (50 ml) and the solution cooled to 0° C. Ethyl chloroformate (6.9 ml, 72.2 mmol) was added slowly and the suspension stirrred for ˜30 mins at 0° C., and for ˜3 hrs at room temperature. Water (150 ml) was added and the mixture extracted with diethyl ether (150 ml). The extracts were washed with water (2×150 ml) and saturated aqueous sodium chloride solution (100 ml). The solution was dried over anhydrous magnesium sulphate and concentrated to give 4-benzyl-benzene-1,3-diol as a pale green gum, solidified on standing, (8.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07247734B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-e821e0afc2624c2286c004b19bbcfb25 |
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| Source note | uspto-grants-2007_07 |
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