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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166446Generated: October 28, 2026

Ammonium Chloride → trans-Cyclohexanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester

https://huagongshe.com/reaction/1166446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodiumHCID 5360545—
ReactantSodium MethoxideHCID 10942334—
ReactantCyclohexanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl ester, (1s,2r)-HCID 11253896—
SolventMethanolHCID 887—
Producttrans-Cyclohexanecarboxylic acid, 2-[[(1,1-dimethylethoxy)carbonyl]amino]-, methyl esterHCID 1077753864.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium metal (0.14 g, 6.1 mmol) was placed into a flame dried flask under nitrogen atmosphere and cooled to 0° C. 10 mL of freshly distilled methanol was added and the mixture stirred until all the sodium dissolved. An amount of 25 (2.00 g, 7.7 mmol) was dissolved in 10 mL of freshly distilled methanol and transferred to NaOMe solution via cannula. The solution was refluxed under nitrogen for 5.5 h, cooled to rt and acidified with 0.5 M aqueous 0.5 M ammonium chloride (18 mL, 9 mmol). The methanol was removed under reduced pressure, and the resulting solid collected by filtration to yield 1.27 g of desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613876B1
Source datasetuspto-grants-2003_09
ORD IDord-32e4d0cbc47344faa24508f9dfb3aa50
Source noteuspto-grants-2003_09