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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374885Generated: October 30, 2026

Acetic Anhydride → (2R)-[(benzyloxyformylamino)methyl]heptanoic acid

https://huagongshe.com/reaction/1374885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant(R)-3-Benzyloxyamino-2-pentylpropionic acidHCID 86592156—
SolventFormic AcidHCID 284—
SolventDichloromethaneHCID 6344—
Product(2R)-[(benzyloxyformylamino)methyl]heptanoic acidHCID 66603339189.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold solution of (R)-3-Benzyloxyamino-2-pentylpropionic acid (1.03 g, 3.89 mmol) in HCO2H (19 mL) and dichloromethane (19 mL) at 0° C. was added acetic anhydride (3.9 mL, 41.2 mmol). The mixture was stirred at 0° C. for 3 hours. The volatiles were removed by evaporation under vacuum. Dichloromethane (50 mL) was added to it. It was washed with brine (50 mL×2), and dried over MgSO4. Filtration and evaporation under vacuum provided the title compound (1.08 g, 95%). 1H NMR (400 MHz, CHCl3) δ 8.07 (br s, 1H), 7.29 (m, 5H), 4.91–4.71 (m, 2H), 3.76 (m, 2H), 2.67 (m, 1H), 1.54 (m, 1H), 1.41 (m, 1H), 1.20 (m, 6H), 0.80 (t, J=7.0 Hz, 3H). Mass spectrum ES+: 294 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166624B2
Source datasetuspto-grants-2007_01
ORD IDord-b6a7e5f711924a3f973ec22d77ec25cf
Source noteuspto-grants-2007_01