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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496228Generated: October 26, 2026

Methanol → Phenstatin Acetate

https://huagongshe.com/reaction/496228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantPhenstatinHCID 9948888—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductPhenstatin AcetateHCID 86759841—

Reaction Steps

Acetic anhydride (74 μL, 0.79 mmol) was added to a solution of phenstatin (3b, 0.2 g, 0.63 mmol), DMAP (7.8 mg, 0.063 mmol) and triethylamine (0.13 mL, 0.94 mmol) in dry methylene chloride (1.5 mL, under argon at room temperature). The yellow solution was stirred for 30 min (reaction was complete by TLC). Methanol (5 Ml) was added and the reaction mixture concentrated to a solid that was washed with diethyl ether (3 ×10 mL) and partitioned between ethyl acetate and cold Ln hydrochloric acid. The organic layer was washed with 10% aqueous sodium bicarbonate and dried. Solvent removed, in vacuo, gave an off-white solid that was recrystallized from ethyl acetate-hexane to give colorless snowflakes of analytical purity: EIMS m/z (peak height) 360 M+, 60%), 318 (100%), 303 (10%), 195 (20%), 151 (30%), 91 (32%), 44 (25%). 1H-NMR (CDCl3)δ H 7.740 (1H, dd, J6/2 2.1 Hz, J6/5 8.1 Hz, H-6). 7.556 (1H, d, J2/6 2.1 Hz, H-2), 7.026 (1H, d, J5/6 8.0 Hz, H-5), 7.013 (2H, s, H-2′, 6′), 3.914 (3H, s, 4-OCH3), 3.907 (3H, s, 4′-OCH3), 3.863 (6H, s, 3′, 5′-OCH3), 2.315 (3H, s, —OCOCH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06943194B1
Source datasetuspto-grants-2005_09
ORD IDord-047a20263ceb4b9bb1e7157a4a00eabd
Source noteuspto-grants-2005_09