Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trichloroethylene | HCID 6575 | — |
| Reactant | HCID 86738645 | HCID 86738645 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 86738644 | HCID 86738644 | — |
Reaction Steps
3.3 g of 1,6-dipalmitoyl-D-mannitol and 0.53 of benzene boronic acid anhydride was added to a solution containing 20 ml of pyridine and 20 ml of trichloroethylene, and the mixture was dried with 5 g of molecular sieves. The mixture was cooled at -18° C. and 3.3 g of oleoyl chloride, dissolved in 10 ml of trichloroethylene, was added. The mixture was left standing over night at -18° C. and for four hours at room temperature. The reaction mixture was washed with 120 ml of 2 N hydrochloric acid and with water, and fractionated in a column containing 160 g of Sephadex LH 20 and eluting with a 1:1-mixture of chloroform and ethanol (90%), whereby the boronic acid protection was removed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04360694 |
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| Source dataset | uspto-grants-1982_11 |
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| ORD ID | ord-6d72e4e5176046ba99170cf11857195d |
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| Source note | uspto-grants-1982_11 |
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