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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796839Generated: October 30, 2026

Hydrochloric Acid → 1-(aminomethyl)spiro[2.5]octane-1-carboxylic Acid Hydrochloride

https://huagongshe.com/reaction/1796839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactant1-(((tert-Butoxycarbonyl)amino)methyl)spiro[2.5]octane-1-carboxylic acidHCID 11818423—
Solvent1,4-DioxaneHCID 31275—
Product1-(aminomethyl)spiro[2.5]octane-1-carboxylic Acid HydrochlorideHCID 1022008286%

Reaction Steps

To a solution of 1-(tert-butoxycarbonylamino-methyl)-spiro[2.5]octane-1-carboxylic acid (200 mg, 0.706 mmol) in 1,4-dioxane (3 mL) was added 4N HCl in 1,4-dioxane (3 mL). The reaction was stirred for 18 hours at room temperature. Ether (20 mL) was added and the precipitate was isolated by vacuum filtration. The solid was dried in a vacuum oven at 48° C. to give 133 mg (86%) of 1-aminomethyl-spiro[2.5]octane-1-carboxylic acid hydrochloride as a white solid: mp 240–242° C.; 1H NMR (300 MHz, D2O) δ 0.92 (d, J=5.2 Hz, 1H), 1.40 (d, J=5.2 Hz, 1H), 1.4–1.6 (m, 10H), 3.12 (d, J=14.0 Hz, 1H), 3.61 (d, J=14.0 Hz, 1H); MS (APCI) m/z 184 [M+H]+. Anal. Calcd. For C10H17NO2—HCl: C, 54.67; H, 8.26; N, 6.38; Cl, 16.14. Found: C, 54.91; H, 8.36; N, 6.25; Cl, 15.99.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030267B2
Source datasetuspto-grants-2006_04
ORD IDord-e5361dab4f824e35870598745f567a21
Source noteuspto-grants-2006_04