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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363897Generated: October 30, 2026

Acetyl chloride → (+)-O-Acetyl-D-malic Anhydride

https://huagongshe.com/reaction/2363897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantD-Malic acidHCID 92824—
Product(+)-O-Acetyl-D-malic AnhydrideHCID 9815264—

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of D-malic acid (10 g, 75 mmol, Major Chemicals Co. Ltd. lot #KS00404) in acetyl chloride (30 mL, Aldrich cat #11, 418-9) was heated to 45° C. for 6 h. The excess acetyl chloride was evaporated in vacuo and the residue was taken up in dichloromethane (10-15 mL). The volatiles were removed in vacuo and the residual oil was stored at 4° C. for 18 h. Under cold storage, the oil crystallized, giving rise to (R)-(+)-2-acetoxysuccinic anhydride (95a) as a white solid (11.7 g, quant yield); m.p. 52° C.; [α]D+23.82° (c 5.44, acetone); 1H-NMR (300 MHz, CDCl3) δ: 5.51 (dd, 1H, J 6 Hz, 9 Hz), 3.36 (dd, 1H, J 19 Hz, 9 Hz), 3.00 (dd, 1H, J 19 Hz, 6 Hz), 2.17 (s, 3H); 13C-NMR (75 MHz, CDCl3) δ: 169.61 (+), 167.66 (+), 166.21 (+), 67.51 (−), 35.10 (+), 20.16 (−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08692002B2
Source datasetuspto-grants-2014_04
ORD IDord-97b28ee8ed7d4473b37c9f906d3cd4cd
Source noteuspto-grants-2014_04