Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 12630295 | HCID 12630295 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12901376 | HCID 12901376 | 69.9% |
Reaction Steps
A mixture of 8 g (30 mmoles) of 2-(ethoxycarbonyl)ethyltrimethylstannane (compound 47), 5 ml of 95% hydrazine (150 mmoles) in 10 ml of ethanol was refuxed for 2 hours. The volatiles were removed at reduced pressure. Distillation of the crude product afforded 5.26 g of 2-(hydrazinocarbonyl)ethyltrimethylstannane, b.p. 92°-98° C. (0.07 mm), compound 42 of Table I. The infrared spectrum of the distillate showed the following characteristic absorptions: 3300 cm-1 (N-H), 1660 cm-1 and 1530 cm-1 ##STR21## and 760 cm-1 (--Sn(CH3)3). A gas chromatogram of the sample showed a single peak on a 6 feet × 1/8 inch commercially obtained column packed with 10% of silicone gum rubber on silanized diatomaceous earth. The NMR spectrum exhibited the following proton absorptions: a broad singlet at 752 Hz (1 proton) assigned to N-H, a singlet at 388 Hz (2 protons) assigned to NH2, a triplet centered at 235 Hz (2 protons) assigned to ##STR22## a triplet centered at 98 Hz (2 protons) assigned to CH2 -Sn, and a singlet centered at 6 Hz (9 protons) assigned to Sn(CH3)3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04160846 |
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| Source dataset | uspto-grants-1979_07 |
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| ORD ID | ord-fa97120a38ca4c84b505cfcdbc54a478 |
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| Source note | uspto-grants-1979_07 |
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