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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628094Generated: October 31, 2026

Hydrochloric Acid → 4-([(9H-Fluoren-9-ylmethoxy)carbonyl]amino)-4-methylpentanoic acid

https://huagongshe.com/reaction/1628094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium CarbonateHCID 10340—
Reactant9-Fluorenylmethyl chloroformateHCID 34367—
Reactant4-Amino-4-methylpentanoic acidHCID 228069—
Solvent1,4-DioxaneHCID 31275—
Product4-([(9H-Fluoren-9-ylmethoxy)carbonyl]amino)-4-methylpentanoic acidHCID 5838211849.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred solution containing 4-amino-4-methylpentanoic acid (0.90 g, 6.86 mmol, Chembridge), Na2CO3 (2.9 g, 27. mmol), and 1,4-dioxane (10 mL) was cooled in an ice bath and Fmoc-Cl (2.1 mg, 8.2 mmol) dissolved in 1,4-dioxane (10 mL) was added in over about 2 min. The mixture was stirred at about 0° C. for about 1 h and then allowed to warm to rt. The mixture was neutralized with aqueous 6 N HCl and extracted with EtOAc (3×25 mL). The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure. The crude material was purified by flash chromatograph (40 g silica gel column, 10-60% EtOAc/Heptane) to give 4-(((9H-fluoren-9-yl)methoxy)carbonylamino)-4-methylpentanoic acid the title compound (1.2 g, 49%): LC/MS (Table 2, Method b) Rt=2.31 min.; MS m/z: 352 (M−H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785639B2
Source datasetuspto-grants-2014_07
ORD IDord-1e4f452c56214c83b58404e50e6308d1
Source noteuspto-grants-2014_07