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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339630Generated: October 30, 2026

Acetic Anhydride → HCID 68646139, compound

https://huagongshe.com/reaction/339630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 68646043HCID 68646043—
SolventDichloromethaneHCID 6344—
ProductHCID 68646139HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895534B2
Source datasetuspto-grants-2014_11
ORD IDord-fa655d7e244f4d1a98a03a709d0e9065
Source noteuspto-grants-2014_11