HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 68646139, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 68646043 | HCID 68646043 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68646139 | HCID 68646139 | — |
Reaction Steps
Ac2O (1.16 mL, 12.3 mmol) was added slowly to a solution of Et3N (2.33 mL, 16.5 mmol) and 7-(3-amino-propoxy)-3-nitromethyl-3H-benzo[c][1,2]oxaborol-1-ol hydrochloride (1.69 g, 76.5 mmol) in CH2Cl2 (50 mL) at 0° C. (bath temp). The reaction mixture was stirred at rt for 1 h and then quenched with H2O (50 mL). The mixture was extracted with CH2Cl2 and the organic fraction was dried (MgSO4) and concentrated in vacuo to give the title compound as a viscous liquid: yield 1.29 g (75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895534B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-fa655d7e244f4d1a98a03a709d0e9065 |
| Source note | uspto-grants-2014_11 |