HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Thionyl Chloride → 10-Chloro-1-decene

HRID 1199866
Notes
Print preview

Reaction equation

HRID 1199866 reaction equation
[CH2:1](O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH:9]=[CH2:10].S(Cl)([Cl:14])=O>N1C=CC=CC=1.ClCCl>[Cl:14][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH:9]=[CH2:10]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 24386Thionyl ChlorideHCID 256129-Decen-1-ol

Product 1

HCID 1174513910-Chloro-1-deceneYield 95.3%

Reagents, catalysts & solvents 2

HCID 1049PyridineCatalystHCID 6344DichloromethaneSolvent

Procedure

To 26.0 g of 9-decene-1-ol was added 10-drops of pyridine and the mixture was placed into an eggplant flask. To the eggplant flask was added dropwise 24.0 g of thionyl chloride during cooling with ice. After dropping, the mixture was reacted for 8.5 hours at 70° C. After the conclusion of the reaction, the reaction product was diluted with dichloromethane and then washed with an aqueous potassium carbonate solution. The reaction solution was then dried over magnesium sulfate and subsequently concentrated under reduced pressure. The resulting residue was purified by column chromatography to obtain 27.7 g of 10-chloro-1-decene. (Yield: 95%)

Workup

  1. customthe mixture was placed into an eggplant flask
  2. temperatureduring cooling with ice
  3. customthe mixture was reacted for 8.5 hours at 70° C
  4. customAfter the conclusion of the reaction
  5. washwashed with an aqueous potassium carbonate solution
  6. dry with materialThe reaction solution was then dried over magnesium sulfate
  7. concentrationsubsequently concentrated under reduced pressure
  8. customThe resulting residue was purified by column chromatography

Sources & evidence

ORD record
ord-f1bc5469004c4bc2ac4b6826801d7aaa
Source dataset
uspto-grants-1990_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04904065

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes