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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788828Generated: October 26, 2026

Acetic Anhydride → N-Benzyloxycarbonyl 2-chloro-4,5-diacetoxyphenylglycine

https://huagongshe.com/reaction/1788828

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium CarbonateHCID 10340—
ReactantN-Benzyloxycarbonyl 2-chloro-4,5-dihydroxyphenylglycineHCID 54341029—
SolventWaterHCID 962—
ProductN-Benzyloxycarbonyl 2-chloro-4,5-diacetoxyphenylglycineHCID 53660034—

Reaction Steps

N-Benzyloxycarbonyl 2-chloro-4,5-dihydroxyphenylglycine (1.76 g, 5 mmole) in water (30 ml) and THF (20 ml) was adjusted to pH 7.5 with saturated sodium carbonate solution. Acetic anhydride (1.2 ml) was added and pH 6.5 maintained with saturated sodium carbonate solution, after 15 minutes and again after a further 15 minutes more acetic anhydride (0.6 ml) was added. After another 15 minutes the solution was washed with ether (2×25 ml), acidified to pH 2.5 and extracted with ethyl acetate (3×30 ml). The extracts were washed with water (2×25 ml) and brine (20 ml) dried and evaporated to a foam, 1.87 g 86%, δ[(CD3)2CO] 2.20(6H, s, 2×OCOCH3), 5.03(2H, s, OCH2), 5.80(1H, d, J8 Hz, CHNH), 7.12(1H, d, J8 Hz, CHNH), 7.23(5H, s, Ph), 7.33 and 7.35(2H, 2×s, Ar), 9.57(1H, s, CO2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04684639
Source datasetuspto-grants-1987_08
ORD IDord-f891e300ccd949b285d97d069a945d6c
Source noteuspto-grants-1987_08