Reaction #4166567
Related Literature (1)
openreactiondata ↗doi:10.1039/C8SC04228D
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-10b1084dbf374e78bc31a98aa6ec9aa3No renderable structure data available
C(CCCCCC#N)CCCCCOChemical Intermediate
Structures, identifiers and computed properties have been matched to the database record by CAS.
| Intermediates | 12-hydroxydodecanenitrile |
|---|---|
| IUPAC Name | — |
| CAS Number | 73782-16-8 |
| Database ID | 10330348 |
| Molecular Formula | — |
| Molecular Weight | — |
Product Information
12-hydroxydodecanenitrile (CAS 73782-16-8) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
Potential Applications
For professional research and industrial use only
Database ID 10330348
Safety Notice
For professional research and industrial use only. Review the supplier safety data sheet before handling.
Synthesis data
11 reactions · 11 references
Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-10b1084dbf374e78bc31a98aa6ec9aa3Conditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-ce79e6229f7d4bb4b7ed71818189c02eConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-10b1084dbf374e78bc31a98aa6ec9aa3Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution of 15 g. of 12-hydroxydodecanonitrile and 14 ml. of triethylamine in 320 ml. of methylene chloride is stirred at 0° C. while 5.7 ml. of methanesulfonylchloride is added dropwise. The mixture is stirred at 0° C. for 1 hour, diluted with methylene chloride and extracted with water; cold, dilute hydrochloric acid; saturated aqueous sodium bicarbonate; and brine. The solution is dried over anhydrous magnesium sulfate and eaporated to yield 12-(methanesulfonyloxy)dodecanonitrile as a yellow oil extracted with water The solution is dried over anhydrous magnesium sulfate
Source ID: ord-e37a4953a573467f99662f7bda5b71b2Conditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution of 15 g. of 12-hydroxydodecanonitrile and 14 ml. of triethylamine in 320 ml. of methylene chloride is stirred at 0° C. while 5.7 ml. of methanesulfonylchloride is added dropwise. The mixture is stirred at 0° C. for 1 hour, diluted with methylene chloride and extracted with water; cold, dilute hydrochloric acid; saturated aqueous sodium bicarbonate; and brine. The solution is dried over anhydrous magnesium sulfate and eaporated to yield 12-(methanesulfonyloxy)dodecanonitrile as a yellow oil extracted with water The solution is dried over anhydrous magnesium sulfate
Source ID: ord-e37a4953a573467f99662f7bda5b71b2Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution 4.6 g. of 11-bromoundecanol and 1.6 g. of sodium cyanide in 40 ml. of dimethylformamide is heated at 80° C. for 18 hours, cooled, and poured into ice-water. The mixture is extracted with methylene chloride and the extract is dried over anhydrous magnesium sulfate. Evaporation of the solution affords 12-hydroxydodecanonitrile as a yellow oil. cooled The mixture is extracted with methylene chloride the extract is dried over anhydrous magnesium sulfate Evaporation of the solution
Source ID: ord-af4d2d2762314fcc986794205f24620bConditions: temp:0.00; pressure:0.00; stir:
Source ID: ord-ce79e6229f7d4bb4b7ed71818189c02eConditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution of 15 g. of 12-hydroxydodecanonitrile and 14 ml. of triethylamine in 320 ml. of methylene chloride is stirred at 0° C. while 5.7 ml. of methanesulfonylchloride is added dropwise. The mixture is stirred at 0° C. for 1 hour, diluted with methylene chloride and extracted with water; cold, dilute hydrochloric acid; saturated aqueous sodium bicarbonate; and brine. The solution is dried over anhydrous magnesium sulfate and eaporated to yield 12-(methanesulfonyloxy)dodecanonitrile as a yellow oil. extracted with water The solution is dried over anhydrous magnesium sulfate
Source ID: ord-1f55e391ef3a4461bb29f43c924e8beaConditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution 4.6 g. of 11-bromoundecanol and 1.6 g. of sodium cyanide in 40 ml. of dimethylformamide is heated at 80° C. for 18 hours, cooled, and poured into ice-water. The mixture is extracted with methylene chloride and the extract is dried over anhydrous magnesium sulfate. Evaporation of the solution affords 12-hydroxydodecanonitrile as a yellow oil. cooled The mixture is extracted with methylene chloride the extract is dried over anhydrous magnesium sulfate Evaporation of the solution
Source ID: ord-1d9be8fa42bd4aa28b64c51da6d1f1bcConditions: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution of 15 g. of 12-hydroxydodecanonitrile and 14 ml. of triethylamine in 320 ml. of methylene chloride is stirred at 0° C. while 5.7 ml. of methanesulfonylchloride is added dropwise. The mixture is stirred at 0° C. for 1 hour, diluted with methylene chloride and extracted with water; cold, dilute hydrochloric acid; saturated aqueous sodium bicarbonate; and brine. The solution is dried over anhydrous magnesium sulfate and eaporated to yield 12-(methanesulfonyloxy)dodecanonitrile as a yellow oil extracted with water The solution is dried over anhydrous magnesium sulfate
Source ID: ord-e37a4953a573467f99662f7bda5b71b2Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: A solution 4.6 g. of 11-bromoundecanol and 1.6 g. of sodium cyanide in 40 ml. of dimethylformamide is heated at 80° C. for 18 hours, cooled, and poured into ice-water. The mixture is extracted with methylene chloride and the extract is dried over anhydrous magnesium sulfate. Evaporation of the solution affords 12-hydroxydodecanonitrile as a yellow oil. cooled The mixture is extracted with methylene chloride the extract is dried over anhydrous magnesium sulfate Evaporation of the solution
Source ID: ord-af4d2d2762314fcc986794205f24620bPubChem References
These sources are listed in the compound's public database record.
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