Reaktion #1370898

ord-20b5c85934414fbda743cf188af9e309

Reaktionsgleichung

O=C(O)CCC(=O)NCCc1cccc2ccccc12
NESA
O=C(O)CCC(=O)NCCc1cccc2ccccc12
NESA
O=C1c2cc([N+](=O)[O-])ccc2-c2c1cc([N+](=O)[O-])cc2[N+](=O)[O-]
2,4,7-trinitro-9-fluorenone
→
CCCCCCCCC(C)C
Isopar G

Edukte

O=C(O)CCC(=O)NCCc1cccc2ccccc12
NESA
O=C(O)CCC(=O)NCCc1cccc2ccccc12
NESA
—
layer 13
O=C1c2cc([N+](=O)[O-])ccc2-c2c1cc([N+](=O)[O-])cc2[N+](=O)[O-]
2,4,7-trinitro-9-fluorenone

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

One half of the exposure zone (5.7 cm. by 5.7 cm.) of NESA glass plate 12 was coated with a 20 micron thick layer of a dark charge exchange layer 13 composed of 2,4,7-trinitro-9-fluorenone and a Butvar binder as described in the formulation given in Example 6. The other half of the NESA glass plate 12 was left uncoated.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US03976485uspto-grants-1976_08