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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765985Generated: October 29, 2026

HCID 17851043, compound → HCID 54030461, compound

https://huagongshe.com/reaction/1765985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 17851043HCID 17851043—
CatalystCobalt(II) chlorideHCID 24288—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 54030461HCID 5403046137.1%

Reaction Conditions

Temperature37 °C

Reaction Steps

In a mixture of water (36.5 ml) and 1N sodium hydroxide solution (29 ml) was dissolved N-acetyl-3-methoxy-4-methyl-DL-phenylalanine (7.28 g). Cobalt chloride (II) hexahydrate (36.5 mg) and acylase (Acylase Amano 36.5 mg) were added to the solution and the mixture was stirred at 37° C. for 15.5 hours while adjusting pH of the reaction mixture to 7.5 with 1N sodium hydroxide solution. Insoluble matters were removed by filtration and pH of the filtrate was adjusted to 3 with 6N hydrochloric acid. After extraction with ethyl acetate, the extract was washed with water, dried over sodium sulfate and the solvent was evaporated under vacuum to give crude N-acetyl-3-methoxy-4-methyl-D-phenylalanine (3.17 g). The crude product was subjected again to the acylase reaction (15.2 mg cobalt chloride (II) hexahydrate, 152 mg acylase, 37° C., pH 7.5, 20 hours) to give pure N-acetyl-3-methoxy-4-methyl-D-phenylalanine (2.70 g) in the form of a viscous oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07229992B2
Source datasetuspto-grants-2007_06
ORD IDord-29ce840310b54b7aa04277168bdd53ea
Source noteuspto-grants-2007_06