Tetrahydrofuran → HCID 71477884, compound

HRID 1523012Notes

Reaction equation

HRID 1523012 reaction equation
C([S:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13](=[C:19]([CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][S:33]C(=O)C)[CH2:20][C:21](OC)=[O:22])[CH2:14][C:15](OC)=[O:16])(=O)C.C1COCC1.CC(C[AlH]CC(C)C)C>C1(C)C=CC=CC=1>[SH:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12]/[C:13](=[C:19](\[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][SH:33])/[CH2:20][CH2:21][OH:22])/[CH2:14][CH2:15][OH:16]

Participants

5

Procedure

To a flamed-dried 20 mL vial fitted with a screw-cap septa was added Dimethyl 3,4-bis(8-(acetylthio)octyl)hex-3-enedioate (1 equiv, 0.36 mmol, 196 mg) and THF (4.5 mL). DIBAl-H (12 equiv, 4.3 mmol, 2.9 mL of a nominally 1.5 M solution in toluene) was added dropwise at rt. The reaction was stirred at rt for 2 h and quenched by the careful addition of 2N HCl (3 mL). The solution was transferred to a sepratory funnel and diluted with sat. aq. NH4Cl (15 mL) and Et2O (15 mL). The layers were separated and the aqueous layer extracted with Et2O (2×15 mL). The combined organic layers were washed with brine (20 mL), dried with Na2SO4, concentrated in vacuo, and purified by flash column chromatography (40% EtOAc/Hex) to afford (Z)-3,4-bis(8-mercaptooctyl)hex-3-ene-1,6-diol (82.8 mg, 0.205 mmol, 57%). TLC Rf=0.41 (50% EtOAc/Hex); Mp=67.4-68.2° C.; 1HNMR (600 MHz): δ 3.64 (t, 4H, J=6.9 Hz), 2.54 (q, 4H, J=7.4 Hz), 2.35 (t, 4H, J=7.0 Hz), 2.08-2.02 (4H), 1.68 (bs, 2H), 1.62 (quint., 4H, J=7.4 Hz), 1.42-1.27 (22H); 13CNMR (150 MHz): δ 132.4, 61.3, 34.6, 34.0, 31.7, 29.7, 29.5, 29.2, 29.0, 28.3, 24.6; FTIR: 3402, 3349, 2923, 2850, 1465, 1348, 1028, 721 cm−1; HRMS-ESI: calc. for C22H44NaO2S2 (M+Na)+: 427.2680. found: 427.2679.

Workup

  1. customTo a flamed-dried 20 mL vial fitted with a screw-cap septa
  2. customquenched by the careful addition of 2N HCl (3 mL)
  3. customThe solution was transferred to a sepratory funnel
  4. additiondiluted with sat. aq. NH4Cl (15 mL) and Et2O (15 mL)
  5. customThe layers were separated
  6. extractionthe aqueous layer extracted with Et2O (2×15 mL)
  7. washThe combined organic layers were washed with brine (20 mL)
  8. dry with materialdried with Na2SO4
  9. concentrationconcentrated in vacuo
  10. custompurified by flash column chromatography (40% EtOAc/Hex)

Sources & evidence

ORD record
ord-25cbe1ceb83c47578b2758eeb9c847d0
Source dataset
uspto-grants-2015_07
Patent number
US09079835B2

Reaction notes

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