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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536778Generated: October 30, 2026

Chloroform → HCID 130126346, compound

https://huagongshe.com/reaction/536778

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantHCID 46184189HCID 46184189—
SolventWaterHCID 962—
ProductHCID 130126346HCID 130126346—

Reaction Steps

(S)-8-(4S,5S)-5-heptyl-2,2-dimethyl-1,3-dioxolan-4-yl)octa-1-en-4,6-diyn-3-ol, ent-panaxytriol acetonide was prepared from (3S,9S,10S)-heptadeca-1-en-4,6-diyne-3,9,10-triol, ent-panaxytriol, by the method described in Yun, H.; Chou, T. C.; Dong, H.; Tian, Y.; Li, Y-M.; Danishefsky, S. J. J. Org Chem. 2005, 70, 10375, yielding the product with: [α]19.3D-70.5 (c=0.13, CHCl3). 1H NMR (300 MHz, CDCl3) δ 5.94 (ddd, 17.1 Hz, 10.2 Hz, 5.4 Hz, 1H), 5.47 (d, 17.1, 1H), 5.26 (d, 10.2 Hz, 1H), 4.92 (d, 5.1 Hz, 1H), 4.36 (t, 6 Hz, 1H), 3.77 (m, 2H), 2.60 (m, 2H), 1.7-1.2 (m, 12H), 1.40 (s, 6H), 0.88 (t, 6.9 Hz, 3H). LRMS (APCI+) found 319.0, [M]+, 333.04, [M+H2O]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859615B2
Source datasetuspto-grants-2014_10
ORD IDord-911b7286c17147909c967582309245e6
Source noteuspto-grants-2014_10