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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648700Generated: October 30, 2026

Water → HCID 14127334, compound

https://huagongshe.com/reaction/648700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 14127331HCID 14127331—
SolventMethanolHCID 887—
ProductHCID 14127334HCID 14127334—

Reaction Steps

To a suspension of 2.0 g of methyl 2-(3-chloropropyl)-3-oxo-2,3,4,5-tetrahydro-1-benzoxepin-2-carboxylate obtained in Reference Example 1 in 30 ml of methanol, sodium borohydride is added in small portions with stirring and under ice-cooling. After completion of the reaction, the reaction mixture is treated with water and extracted with ethyl acetate. The organic layer is washed with water, dried, and evaporated under reduced pressure. The residue is purified by column chromatography on silica gel (eluant: hexane:ethyl acetate=3:1→1:1). From the first fraction eluted, methyl 2-(3-chloropropyl)-3-hydroxy-2,3,4,5-tetrahydro-1-benzoxepin-2-carboxylate (A isomer) is obtained as a colorless oil. Mass spectrum m/e: 298, 300 (M+). IR νmaxneat cm-1 : 3500 (OH), 1735. NMR(CDCl3) δ: 2.0 (6H, multiplet), 3.0(2H, multiplet), 3.5 (2H, triplet, ClCH2 --), 3.70 (3H, s, OCH3), 4.18 (1H, multiplet, C3 --H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04736031
Source datasetuspto-grants-1988_04
ORD IDord-c71fa7b5b16b46ad8158abcfdf2f7574
Source noteuspto-grants-1988_04