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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284879Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 70465999, compound

https://huagongshe.com/reaction/1284879

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 57222703HCID 57222703—
ReactantHCID 57289156HCID 57289156—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
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 extraction) 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 numberUS04564474
Source datasetuspto-grants-1986_01
ORD IDord-f730f1dfd7de412285030c86c807a40e
Source noteuspto-grants-1986_01