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1-Tridecyne → HCID 53669740, compound

HRID 986545
Notes
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Reaction equation

HRID 986545 reaction equation
Br[C:2]1[CH:13]=[CH:12][C:5]([CH:6]=[CH:7][C:8]([O:10][CH3:11])=[O:9])=[CH:4][CH:3]=1.[CH:14]#[C:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]>C(N(CC)CC)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[C:14]([C:2]1[CH:13]=[CH:12][C:5]([CH:6]=[CH:7][C:8]([O:10][CH3:11])=[O:9])=[CH:4][CH:3]=1)#[C:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 2

HCID 1177541-TridecyneHCID 8167732-Propenoic acid, 3-(4-bromophenyl)-, methyl ester

Product 1

HCID 53669740HCID 53669740, compoundYield 47%

Reagents, catalysts & solvents 3

HCID 11776TriphenylphosphineCatalystHCID 167845palladium(II) acetateCatalyst
HCID 8471
Triethylamine
Solvent

Procedure

To a deaerated solution of methyl 4-bromocinnamate (9.64 g, 40 mmole) in dry triethylamine (120 ml) was added triphenylphosphine (308 mg) followed by 1-tridecyne (8.00 g, 45 mmole) and palladium (II) acetate (92 mg) under nitrogen. The mixture was heated to reflux for 24 hours, the reaction being followed by hplc. After this time the mixture was cooled and the precipitated triethylamine hydrobromide was filtered off and washed with a little triethylamine. The filtrate was evaporated to a red solid which was chromatographed on 220 g of silica eluting with petroleum ether [bp 60-80]-dichloromethane (3:2) to give 6.26 g (47%) of title compound as a pale yellow solid of mp (MeOH) 57°-59° C., υmax (mull) 1710, 1630, 1600, 1315, 1170, 1000, 830 cm-1, δ(CDCl3). 0.85 (3H, distorted t, terminal CH3), 1.28 (18H, m, alkylene chain), 2.38 (2 H, t, J 6.5 Hz, C≡C--CH2), 3.78 (3H, s, ester CH3), 6.37 (1H, d, J 16 Hz, =CHCO2), 7.42 (4H, near s, arom), 7.63 (1H, d, J 16 Hz, ArCH=)

Workup

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 24 hours
  3. temperatureAfter this time the mixture was cooled
  4. filtrationthe precipitated triethylamine hydrobromide was filtered off
  5. washwashed with a little triethylamine
  6. customThe filtrate was evaporated to a red solid which
  7. customwas chromatographed on 220 g of silica eluting with petroleum ether [bp 60-80]-dichloromethane (3:2)

Sources & evidence

ORD record
ord-56e8b5ed1ac340ea9a19c868ed210814
Source dataset
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04713486

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes