HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516814Generated: October 27, 2026
Acetyl chloride → (+)-O-Acetyl-D-malic Anhydride
https://huagongshe.com/reaction/516814
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | D-Malic acid | HCID 92824 | — |
| Product | (+)-O-Acetyl-D-malic Anhydride | HCID 9815264 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115081B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-18af8f19171547eb91df3a25aa27221d |
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| Source note | uspto-grants-2015_08 |
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