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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703805Generated: November 2, 2026

Methanol → HCID 53873990, compound

https://huagongshe.com/reaction/703805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantHCID 22669248HCID 22669248—
ReactantSodium NitriteHCID 23668193—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 53873990HCID 5387399015.2%

Reaction Steps

To a cold (0°) solution of N-(3-methoxyphenyl)glycine methyl ester (50 g) in aqueous acetic acid (800 ml) was added dropwise an aqueous solution (200 ml) of sodium nitrite (21.2 g) and the mixture was stirred for 30 min. Methanol (200 ml) was added and the mixture was cooled to -10°. Zinc dust (83.2 g) was added portionwise over 2 h during which time the internal temperature was maintained at -10° to 0° and the mixture was stirred for a further 1 h at 0°. Dichloromethane (800 ml) and water (800 ml) were added and the resulting suspension was filtered. The filtrate was diluted with more water (500 ml) and dichloromethane (500 ml). The phases were separated and the aqueous layer was partitioned with more dichloromethane (2×500 ml). The combined organic extracts were washed with water (3×500 ml) and evaporated in vacuo. The residual oil was treated with 8% sodium bicarbonate (1000 ml) and partitioned with ether (3×700 ml). The combined organic layers were washed with brine (500 ml), dried and evaporated. Purification by FCC eluting with System A (1:1) and then System A (7:3) gave the title compound (8.2 g) as an oil, t.l.c. (System A, 1:1) Rf 0.12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04985427
Source datasetuspto-grants-1991_01
ORD IDord-820487027e2843a6bf5c09c57946fbe6
Source noteuspto-grants-1991_01