Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Methyl carbazate | HCID 80519 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | alpha-Hydroxyacetophenone | HCID 68490 | — |
Reaction Steps
A 100-gallon glass lined kettle equipped with a cooling jacket was charged with 90.5 lbs. of acetophenone, 123 lbs. of methanol and 340 mls. of 98% sulfuric acid. The reactor was cooled to 20° C and the mixture was stirred during the addition of 119 lbs. of bromine that was added incrementally by a gravity fed system at a rate so that the temperature was maintained at between 20°-25° C over a 3-hour period. After the bromination was complete, 37 lbs. of methanol, 240 lbs of water and 112 lbs. of sodium formate were added. The mixture was stirred with agitation overnight at 60° C and after cooling to 40° C a solution of 68 lbs. methyl carbazate in 45 lbs. of a 54:46 methanol-water mixture was added. The reaction mixture was stirred for 2-hours at 40° C to form the carbomethoxy nydrazone of α-hydroxy acetophenone. Thereafter the reaction mixture was allowed to cool to 20° C, was centrifuged, and washed with water on the centrifuge.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04105848 |
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| Source dataset | uspto-grants-1978_08 |
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| ORD ID | ord-3c777ec6682f484f8377f2cc7d343f6f |
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| Source note | uspto-grants-1978_08 |
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