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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756403Generated: October 31, 2026

Methanol → Methyl 3-(6-amino-2,3-dihydrobenz-1,4-oxazin-4-ylmethyl)benzoate

https://huagongshe.com/reaction/1756403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantMethyl 3(6-Hexanamido-2,3-dihydrobenz-1,4-oxazin-4-ylmethyl)benzoateHCID 23365863—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-(6-amino-2,3-dihydrobenz-1,4-oxazin-4-ylmethyl)benzoateHCID 5404800558.5%

Reaction Steps

Lithium hydroxide monohydrate (0.2 g.) in water (5 ml.) was added to a stirred solution of methyl 3-(6-hexanamido-2,3-dihydrobenz-1,4-oxazin-4-ylmethyl)benzoate (ca. 400 mg.) in 1:1 v/v methanol: tetrahydrofuran (10 ml.). When TLC (solvent system 80:20:2 v/v/v toluene:ethyl acetate:acetic acid) indicated complete disappearance of ester, the mixture was diluted with water, filtered to remove any solids, and carefully acidified with 1N hydrochloric acid. The precipitate was isolated by filtration and recrystallized from a mixture of methanol and water to give the title compound (0.176 g., 46% overall yield from amino ester (X)) as an off-white solid, m.p. 167°-171° C. (hemihydrate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05440035
Source datasetuspto-grants-1995_08
ORD IDord-0bf149ba833e4200abe559b2b57e3b99
Source noteuspto-grants-1995_08