HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288361Generated: November 4, 2026
Tributyltin Chloride → HCID 85779503, compound
https://huagongshe.com/reaction/1288361
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin Chloride | HCID 15096 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178506888 | HCID 178506888 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Tetrahydrofuran hexane | HCID 21883165 | — |
| Product | HCID 85779503 | HCID 85779503 | — |
Reaction Steps
Employing the apparatus and procedure of Example I, 100 ml. of an approximately one-molar solution of (N,N-dimethylaminosulfonylmethyl)lithium in hexane-THF solvent was added slowly over a period of 30 minutes to 0.1 mole of tri-n-butyltin chloride dissolved in THF. The temperature at addition was -60° C provided by a dry ice-acetone bath and rose through the addition period to 0° C. Following the complete addition, the reaction mixture was stirred for 2 hours at room temperature (20° C) and hydrolyzed by pouring into an aqueous one-molar ammonium chloride solution. Extraction from the hydrolyzate with ether solvent and purification by vacuum distillation yielded the desired compound, (N,N-dimethylaminosulfonylmethyl)tributyltin. The product, a pale-yellow liquid, had a boiling point of from 158°-160° C/0.1 mm. Hg. Analysis gave 43.8% Carbon and 8.5% Hydrogen compared to the calculated values, respectively, of 43.7% and 8.5%. The assigned structure was confirmed by infrared and proton nuclear magnetic resonance spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03988145 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-994cb39c1c194cccb7ce7296b16049d7 |
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| Source note | uspto-grants-1976_10 |
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