HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355471Generated: October 30, 2026
HCID 131720916, compound → HCID 131720915, compound
https://huagongshe.com/reaction/355471
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 131720916 | HCID 131720916 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 131720915 | HCID 131720915 | — |
Reaction Steps
0.67 g of 1,6-bis-O-(4'-methoxycarbonyl-biphenyl-4-yl)-2,5-O-methylene-D-mannitol was heated under reflux for 16 hours in 15 ml of concentrated sodium hydroxide solution and 15 ml of methanol; thereupon the mixture was evaporated and the residue was acidified with dilute hydrochloric acid. The precipitate of 1,6-bis-O-(4'-carboxy-biphenyl-4-yl)-2,5-O-methylene-D-mannitol which thereby formed was filtered off, dissolved in 5 ml of acetic anhydride and 5 ml of pyridine and stirred at room temperature for 16 hours. Now, the mixture was again evaporated, the residue was poured into dilute hydrochloric acid and the mixture was filtered; there was thus obtained 3,4-di-O-acetyl-1,6-bis-O-(4'-carboxy-biphenyl-4-yl)-2,5-O-methylene-D-mannitol in the form of colorless crystals, MS: m/z 669.4 ([M-H]-).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05830920 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-e5b068f29a2046ebada71ebd1847f9c8 |
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| Source note | uspto-grants-1998_11 |
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