HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 15946647, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 15946646 | HCID 15946646 | — |
| Catalyst | Nickel Dichloride | HCID 24385 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 15946647 | HCID 15946647 | 76% |
Reaction Steps
To a stirred solution of 4 (2.50 g, 4.45 mmol) in MeOH (125 mL) a catalytic amount of NiCl2×6H2O was added followed by portions of NaBH4 (in total 0.34 g, 8.9 mmol) every 10 min until no starting material was observed on TLC (system). Ac2O (3 mL) was added after 50 min and the reaction mixture was diluted with toluene, filtered through a plug of silica and concentrated. The residue was purified by silica gel chromatography to give 5 (1.95 g, 3.4 mmol, 76%). 13C-NMR (CDCl3) 170.4, 169.7, 137.3, 137.0 remaining aromatic C 128.5-127.7, 75.3, 72.6, 72.4, 72.1, 72.0, 67.1, 61.91, 61.8, 61.8, 61.3, 61.2, 48.8, 48.6, 28.5 (d, J=142 Hz), 23.0, 20.6, 16.3, 16.2, 16.1; 31P-NMR (CDCl3) 29.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08062641B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-d9f03763e2064d2184e3cc19c48d6cdb |
| Source note | uspto-grants-2011_11 |