HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539140Generated: October 30, 2026
Hydrochloric Acid → Thioacetic acid S-[(E)-4-((3S,7R,10R,13R,14S)-14-hydroxy-7,13-diisopropyl-10-methyl-5,8,11,16-tetraoxo-1,2-dioxa-6,9,12-triaza-cyclohexadec-3-yl)-but-3-enyl]ester
https://huagongshe.com/reaction/539140
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 25152743 | HCID 25152743 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Thioacetic acid S-[(E)-4-((3S,7R,10R,13R,14S)-14-hydroxy-7,13-diisopropyl-10-methyl-5,8,11,16-tetraoxo-1,2-dioxa-6,9,12-triaza-cyclohexadec-3-yl)-but-3-enyl]ester | HCID 25152962 | 41% |
Reaction Steps
To a solution of 9 (24.7 mg, 0.035 mmol) in CH2Cl2 (1.4 mL) was added triethylsilane (28 μL, 0.175 mmol) followed by the dropwise addition of TFA (0.35 mL, 25% v/v). After stirring for 1 h the reaction mixture was concentrated in vacuo and put under high vacuum for 2 h to give the crude thiol 10. At 0° C. to a solution of thiol 10 in CH2Cl2 (0.45 mL) was added diisopropylethylamine (30 μL, 0.172 mmol) followed by acetyl chloride (2.43 μL, 0.034 mmol) in CH2Cl2 (0.1 mL). After stirring for 2 h 10 min 1M HCl (1 mL) was added followed by EtOAc (10 mL) the layers were separated and the organic layer was washed with sat. brine (10 mL). The organic layer was dried (MgSO4) and concentrated in vacuo. Purification by flash column chromatography (eluent 1:0-98:2-96:4-94:6-92.8 CH2Cl2/MeOH) gave the product 11 (7.3 mg, 0.014 mmol, 41%) as a white solid: Rf 0.47 MeOH/CH2Cl2 (1:9).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865655B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-f73769d8cf8f415c8adc978c2dae6539 |
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| Source note | uspto-grants-2014_10 |
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