Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088359Generated: November 1, 2026

Hydrazine hydrate (1:1) → 9-Fluorenylmethyl carbazate

https://huagongshe.com/reaction/2088359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant9-Fluorenylmethyl chloroformateHCID 34367—
SolventAcetonitrileHCID 6342—
SolventAcetonitrile--water (1/1)HCID 18373917—
Product9-Fluorenylmethyl carbazateHCID 161883—

Reaction Steps

To a well-stirred solution of hydrazine hydrate (19 g, 386 mmol) in 150 mL of CH3CN/H2O (1/1, v/v), a solution of FmocCl (10 g, 38.65 mmol) in 600 mL CH3CN was added dropwise at 0° C. over 2 h. The reaction mixture was then allowed to warm to room temperature and stirred for an additional 12 hours, concentrated in vacuo to 150 mL and filtered to yield the title compound as a white solid, which was washed with water and hexane and dried to a constant weight in vacuo (9.74 g, 99%): mp 172-173° C.; 1H NMR (DMSO) δ 4.08 (brs, 2H), 4.21 (t, J=7.2 Hz, 1H), 4.28 (d, J=7.2 Hz, 2H), 7.32 (t, J=7.4 Hz, 2H), 7.42 (t, J=7.4 Hz, 2H), 7.69 (d, J=7.4 Hz, 2H), 7.89 (d, J=7.4 Hz, 2H), 8.36 (brs, 1H); 13C NMR (DMSO) δ 47.7, 66.7, 121.1 (2C), 126.3 (2C), 128.1 (2C), 128.7 (2C), 141.7 (2C), 144.9 (2C), 159.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435954B2
Source datasetuspto-grants-2013_05
ORD IDord-627e4efc836149ec8bda915fd614ca01
Source noteuspto-grants-2013_05