Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 25152743HCID 25152743—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductThioacetic 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]esterHCID 2515296241%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865655B2
Source datasetuspto-grants-2014_10
ORD IDord-f73769d8cf8f415c8adc978c2dae6539
Source noteuspto-grants-2014_10