Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057321Generated: October 30, 2026

HCID 178486028, compound → HCID 178484792, compound

https://huagongshe.com/reaction/2057321

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178486028HCID 178486028—
ReactantHCID 178486209HCID 178486209—
ProductHCID 178484792HCID 178484792—

Reaction Steps

In analogy to example 32.1, trans-[4-(5-Chloro-pent-1-ynyl)-cyclohexyl]-methyl-carbamic acid tert-butyl ester was converted to trans-[4-(5-Chloro-pent-1-ynyl)-cyclohexyl]-methyl-ammonium trifluoroacetate. The compound was purified by dissolving the salt in water, washing it with Et2O (3×). The water phase was adjusted to pH 8 (with aqueous saturated NaHCO3) and extracted with EtOAc (3×) to give trans-[4-(5-Chloro-pent-1-ynyl)-cyclohexyl]-methyl-amine, MS: 314 (MH+, 1Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335687B2
Source datasetuspto-grants-2008_02
ORD IDord-541ea795272c45f292b581b379a394f0
Source noteuspto-grants-2008_02