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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583530Generated: October 29, 2026

p-Toluenesulfonic acid → HCID 70465999, compound

https://huagongshe.com/reaction/1583530

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 57222703HCID 57222703—
ReactantHCID 57289156HCID 57289156—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
ProductHCID 70465999HCID 7046599996%

Reaction Steps

The THP-ether (13) (26 mg, 0.0498 mmol) in methanol (4 ml) and THP (9) (4 ml) was treated with a catalytic amount of TsOH at room temperature for 1 hr. The usual work-up (ethyl acetate for extraction) gave the crude diol (21.4 mg). This diol was treated with acetic anhydride (1 ml) and pyridine (1 ml) at room temperature for 14 hr. The usual work-up (ethyl acetate for ertraction) gave a crude product, which was applied to a column of silica gel (5 g). Elution with benzene-ethyl acetate (10:1) provided the acetate (14) (23.0 mg, 96%); mp 168°-170° C. (methanol). 1H-NMR δ: 0.82 (3H, s, 18-H3), 1.02 (3H, s, 19-H3), 1.07 (3H, d, J=6 Hz, 21-H3), 1.35 (6H, s, 26-H3 and 27-H 3), 2.03 (3H, s, acetyl), 4.55 (1H, m, 3-H), 5.36 (1H, m, 6-H). High resolution MS Calcd for C27H42F2O (M+ --CH3COOH): 420, 3202. Found: 420, 3206.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04552698
Source datasetuspto-grants-1985_11
ORD IDord-90bb3971efb04074b025354be53ead2f
Source noteuspto-grants-1985_11