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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | N-Benzyloxycarbonyl 2-chloro-4,5-dihydroxyphenylglycine | HCID 54341029 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Benzyloxycarbonyl 2-chloro-4,5-diacetoxyphenylglycine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04684639 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-f891e300ccd949b285d97d069a945d6c |
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| Source note | uspto-grants-1987_08 |
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