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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364103Generated: October 31, 2026

Acetic Anhydride → HCID 11998805, compound

https://huagongshe.com/reaction/1364103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 11998803HCID 11998803—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 11998805HCID 1199880549%

Reaction Steps

To a stirred solution of Example 25 (0.10 g, 0.25 mmol) in DCM (10 mL) was added triethylamine (0.03 g, 0.04 mL, 0.28 mmol), acetic anhydride (0.03 g, 0.03 mL, 0.30 mmol) and a catalytic amount of DMAP. The reaction mixture was stirred at r.t. for 16 h before being diluted with DCM (50 mL) and washed with sat. NaHCO3 solution (2×25 mL) and sat. brine (25 mL). The organic fraction was dried over MgSO4 and concentrated in vacuo. Purification by column chromatography (SiO2, 45:55 EtOAc/hexanes) gave the title compound (0.05 g, 49%) as a white solid. δH(CDCl3) 8.37 (1H, d, J 7.1 Hz), 7.82 (1H, dd, J 6.7 and 2.5 Hz), 7.32 (3H, m), 4.35 (1H, bs), 4.02 (1H, m), 3.82 (1H, d, J 11.9 Hz), 3.48-3.69 (4H, m), 3.31 (1H, m), 3.00 (1H, m), 2.66 (2H, d, J 3.3 Hz), 2.55 (3H, s), 2.34 (2H, s), 1.08 (6H, s). LCMS (ES+) 438.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888344B2
Source datasetuspto-grants-2011_02
ORD IDord-dd1f077c1e584d338c55298dfdfc520d
Source noteuspto-grants-2011_02