Dimethyl Sulfide → HCID 69554694, compound

HRID 428920Notes

Reaction equation

HRID 428920 reaction equation
[Cl:1]N1C(=O)CCC1=O.CSC.O[CH2:13]/[CH:14]=[C:15](/[C:17]1[CH:18]=[C:19]([CH:22]=[CH:23][CH:24]=1)[C:20]#[N:21])\[CH3:16]>ClCCl.[Cl-].[Na+].O>[Cl:1][CH2:13]/[CH:14]=[C:15](/[C:17]1[CH:18]=[C:19]([CH:22]=[CH:23][CH:24]=1)[C:20]#[N:21])\[CH3:16]

Participants

6

Conditions

Temperature
-10 °C

Procedure

To a solution of N-chlorosuccinimide (9.8 g, 73.1 mmol) in dichloromethane (25 ml) at −10° C. was added dropwise over 15 minutes dimethylsulfide (5.4 ml, 73.1 mmol). The mixture was stirred at −10° C. for 30 min, then a solution of 3-[(E)-3-hydroxy-1-methyl-1-propenyl]benzonitrile (from Preparation 33, 11.9 g, 69.6 nlmol) in dichloromethane (20 ml) was added dropwise over 15 minutes at −10° C. The mixture was stirred at 0° C. for 1 h, and was then poured onto saturated brine (50 ml). The layers were separated, and the aqueous layer was extracted with diethyl ether (2×50 ml). The extracts were combined, washed with water (50 ml), dried (MgSO4), filtered and concentrated in vacuo. The crude pale yellow oil (13.1 g, 100%) was used directly in the next step.

Workup

  1. stirringThe mixture was stirred at 0° C. for 1 h
  2. customThe layers were separated
  3. extractionthe aqueous layer was extracted with diethyl ether (2×50 ml)
  4. washwashed with water (50 ml)
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-ced134e915dc4481880164ede319d71a
Source dataset
uspto-grants-2001_11
Patent number
US06313312B1

Reaction notes

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