Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 87452643 | HCID 87452643 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 42634449 | HCID 42634449 | — |
Reaction Steps
Dissolve the compound obtained in Step D (4.38×10−4 mol) in dioxane (25 ml). Place under stirring and then add 37% hydrochloric acid (3.5 ml) and heat at 70° C. After 2 hours, the reaction mixture is poured into water (50 ml). Extract 3 times with ethyl acetate (20 ml). The organic phase is washed with water and then with brine, dried over magnesium sulphate, filtered and concentrated using a rotary evaporator. The oily orange-coloured crude product obtained is chromatographed on a silica column using as eluant a 60/40 n-heptane/ethyl acetate mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288433B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-f53f51092eaa4295b0b6f8de732903c9 |
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| Source note | uspto-grants-2012_10 |
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