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1,4,7,10-Tetraazacyclododecane → Qvd35D4RP3

HRID 66220
Notes
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Reaction equation

HRID 66220 reaction equation
[NH:1]1[CH2:12][CH2:11][NH:10][CH2:9][CH2:8][NH:7][CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[CH3:13]OC(OC)N(C)C>C1C=CC=CC=1>[N:1]12[CH:13]3[N:4]([CH2:5][CH2:6][N:7]3[CH2:8][CH2:9][NH:10][CH2:11][CH2:12]1)[CH2:3][CH2:2]2
ParticipantsProcedureSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 649631,4,7,10-TetraazacyclododecaneHCID 78373Dimethylformamide dimethyl acetal

Product 1

HCID 10702593Qvd35D4RP3

Reagents, catalysts & solvents 1

HCID 241BenzeneSolvent

Procedure

In a manner similar to that of Example 2 (A), 5.00 g (29.1 mmol) of 1,4,7,10-tetraazacyclododecane, 3.46 g of dimethylformamide dimethyl acetal and 50 ml of dry benzene gave 5.00 g of colorless liquid, bp 88.5°-90° (0.30 mm). Analytically pure 1,4,7,10-tetraazatricyclo[5.5.1.04,13 ]tridecane was obtained by distillation of this material through a spinning band column, bp 82°-83° (two fractions) (0.25 mm) One fraction had nD25 = 1.5331. The other fraction was analyzed.

Sources & evidence

ORD record
ord-8cb543ec60764a058d57cf1a2f4aa7b6
Source dataset
uspto-grants-1978_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04130715

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes